FDA 510(k)
Official FDA 510(k) clearances matching watches you set
Monitor official FDA 510(k) device clearance records. Generate source-linked change alerts, landscape reports, and optional exports.
Not FDA warning letters. Not USPTO patents. Not a ClinicalTrials.gov pipeline. You supply watches against public 510(k) data.
from $4.00 / 1,000 FDA 510(k) row ($0.004 per delivered fda-510k-row); $0.20 per FDA clearance change alert; $10.00 per FDA clearance landscape report; $6.00 per FDA clearance export. No Actor Start.
Open FDA 510(k) Device Clearance Landscape Report on Apify
FDA 510(k) Device Clearance Landscape Report, not a neighboring Actor
Use this page for this Actor’s job. Use FDA Warning Letters Scraper for FDA warning-letter pages; Use USPTO Patent Search Scraper for USPTO patent search; Use ClinicalTrials.gov Sponsor Pipeline Scraper for Sponsor study inventory.
| This Actor | FDA Warning Letters Scraper | USPTO Patent Search Scraper | ClinicalTrials.gov Sponsor Pipeline Scraper | |
|---|---|---|---|---|
| Intent | 510(k) clearance landscape and change alerts | FDA warning-letter pages | USPTO patent search | Sponsor study inventory |
| Primary input | watches | search terms | queries | sponsors / conditions |
| What it reads | Official FDA 510(k) public records | FDA warning letters | USPTO public search | ClinicalTrials.gov |
| Primary output | Record, alert, report, and export events | Letter rows | Patent rows | Study rows |
| Not this job | Not FDA warning letters. Not USPTO patents. Not a ClinicalTrials.gov pipeline. You supply watches against public 510(k) data. | Not 510(k) clearance landscape. | Not FDA device clearances. | Not 510(k) device clearances. |
Store ID: taroyamada/fda-510k-device-clearance-landscape-report. Respect source terms, robots.txt, and rate limits.
Use cases
- One product/applicant watch with generateReport off first
- Use initialRunMode baseline_only to seed state
- Turn report/export on after the watch is stable
How is FDA 510(k) Device Clearance Landscape Report different from FDA Warning Letters Scraper and USPTO Patent Search Scraper?
FDA 510(k) Device Clearance Landscape Report (taroyamada/fda-510k-device-clearance-landscape-report): Monitor official FDA 510(k) device clearance records. Generate source-linked change alerts, landscape reports, and optional exports. Not FDA warning letters. Not USPTO patents. Not a ClinicalTrials.gov pipeline. You supply watches against public 510(k) data. FDA Warning Letters Scraper is for FDA warning-letter pages (input search terms; FDA warning letters; Letter rows). Not 510(k) clearance landscape. USPTO Patent Search Scraper is for USPTO patent search (input queries; USPTO public search; Patent rows). Not FDA device clearances. ClinicalTrials.gov Sponsor Pipeline Scraper is for Sponsor study inventory (input sponsors / conditions; ClinicalTrials.gov; Study rows). Not 510(k) device clearances.
What input is required?
Live required fields: watches. Published exampleRunInput is shown below.
| Field | Type | Default | Notes |
|---|---|---|---|
watches |
any[] | [] |
510(k) watches. Bounded saved searches by applicant, product code, device name, medical specialty, review panel, clearance type, decision code, regulation number, or decision date. Required. |
monitorKey |
string | "fda-510k-clearance-watch" |
Monitor key. Stable isolated state namespace for a recurring saved clearance watch. |
initialRunMode |
string enum | "baseline_only" |
Initial run mode. baseline_only stores the first observation with zero rows; emit_backfill emits current matches for an explicit first report. enum: baseline_only, emit_backfill |
generateReport |
boolean | true |
Generate clearance landscape report. Generate one aggregate applicant/product-code/specialty landscape report when new or changed observations are emitted. |
emitRawRows |
boolean | false |
Emit 510(k) rows. Emit one normalized public 510(k) row for each new or changed record. This is the low-priced row event. |
emitExport |
boolean | false |
Generate clearance export. Generate a compact JSON-ready export when new or changed observations are emitted. |
emitUnchanged |
boolean | false |
Emit unchanged observations. Accepted for compatibility, but unchanged observations always remain zero rows and zero charge for billing safety. |
maxRecordsPerWatch |
integer | 100 |
Maximum records per watch. Maximum records requested from openFDA per watch. The official API maximum is 1000. minimum=1 maximum=1000 |
maxChargeUsd |
number | 25 |
Maximum charge USD. Fail closed before pushing any row if planned PPE charges exceed this cap. minimum=0.004 maximum=250 |
openfdaApiKey |
string | empty |
Optional openFDA API key. Optional user-supplied free openFDA key. Leave blank: normal use does not require a key. The key is never written to output or state. |
dryRun |
boolean | false |
Dry run. Return representative event rows without calling openFDA, saving state, or charging PPE events. |
Published Store example run input (omitted fields take schema defaults):
{
"watches": [
{
"id": "diagnostic-imaging-2026",
"productCodes": [
"LLZ"
],
"decisionDateFrom": "2026-01-01",
"decisionDateTo": "2026-12-31"
}
],
"maxRecordsPerWatch": 3,
"maxChargeUsd": 3,
"dryRun": false
}Run FDA 510(k) Device Clearance Landscape Report on Apify
How do dataset, webhook, and dry-run delivery work?
Dataset output is the billable surface when rows are written. See live PPE for which events bill. dryRun true validates or samples without the usual dataset/webhook side effects described on the Store schema. Unchanged runs that write zero default-dataset rows typically charge $0.00 on current PPE.
What does a result contain?
Published README Output Example / Sample Output JSON. Treat README samples as illustrations, not a live coverage guarantee. There is no published output JSON schema on the Store page.
How is FDA 510(k) Device Clearance Landscape Report priced?
Billing is pay per event. The live Store card is from $4.00 / 1,000 FDA 510(k) row ($0.004 per delivered fda-510k-row); $0.20 per FDA clearance change alert; $10.00 per FDA clearance landscape report; $6.00 per FDA clearance export. No Actor Start. Current PPE:
| Event | Price | Emitted when |
|---|---|---|
fda-510k-row (FDA 510(k) row) |
$0.004 | Charged only when a fda 510(k) row row is delivered. |
fda-clearance-change-alert (FDA clearance change alert) |
$0.20 | Charged only when a fda clearance change alert row is delivered. |
fda-clearance-landscape-report (FDA clearance landscape report) |
$10.00 | Charged only when a fda clearance landscape report row is delivered. |
fda-clearance-export (FDA clearance export) |
$6.00 | Charged only when a fda clearance export row is delivered. |
from $4.00 / 1,000 FDA 510(k) row ($0.004 per delivered fda-510k-row); $0.20 per FDA clearance change alert; $10.00 per FDA clearance landscape report; $6.00 per FDA clearance export. No Actor Start.
See FDA 510(k) Device Clearance Landscape Report pricing on Apify
Limits to keep in mind
- watches required
- Public FDA 510(k) only
- Report and export are opt-in
- Not PMA or De Novo full-text dumps unless the live schema says so
- Respect source terms, robots.txt, and rate limits.
Open FDA 510(k) Device Clearance Landscape Report on Apify
Related pages
- FDA Warning Letters Scraper — Not 510(k) clearance landscape.
- USPTO Patent Search Scraper — Not FDA device clearances.
- ClinicalTrials.gov Sponsor Pipeline Scraper — Not 510(k) device clearances.
- Tools