Resource / 13512
unknownUnnamed resource.
Which companies just cleared or got FDA approval for a medical device? Search openFDA device 510(k) clearances and PMA premarket approvals by applicant company, pathway (510k/pma), FDA product code, advisory-committee specialty (e.g. Cardiovascular), applicant state, or decision date (since). Returns the applicant company (entity-resolved where possible), device name, product code, and decision date — a fresh target list for device and component sellers. openFDA public-domain records.
| State | Network | Scheme | Atomic amount | Asset | payTo / untrusted |
|---|---|---|---|---|---|
| active | eip155:8453 | exact | 1250000 | 0x833589fCD6eDb6E08f4c7C32D4f71b54bdA02913 | 0x3873d15CF3209c32aaA8d9AA542164E658567129 |
| active | solana:5eykt4usfv8p8njdtrepy1vzqkqzkvdp | exact | 1250000 | EPjFWdd5AufqSSqeM2qN1xzybapC8G4wEGGkZwyTDt1v | BdcZbENFdEyEUMqv9pnRMUnn1Yyeyo2dCMbYXbJ3LmaB |
All advertised payment options are stored. Base (`eip155:8453`) is the operational network for ranking and canaries; non-Base options remain visible for transparency.
No probe attempts recorded yet. Coverage runs prioritize never-probed endpoints.
Machine contract
Schemas.
{
"method": "GET",
"queryParams": {
"company": "Medtronic",
"pathway": "510k",
"product_code": "DXY"
},
"type": "http"
}
{
"example": {
"rows": [
{
"advisory_committee": "Cardiovascular",
"applicant": "Pacesetter Systems",
"clearance_type": "Traditional",
"date_received": "1985-02-19",
"decision_code": "SESE",
"decision_date": "1985-04-01",
"decision_description": "Substantially Equivalent",
"decision_id": "K850651",
"device_name": "PROGRAMALITH III-3 MODEL 231 PULSE GENERATOR",
"entity_id": null,
"generic_name": null,
"pathway": "510k",
"product_code": "DXY",
"state": "CA"
}
],
"total_matched": 1
},
"type": "json"
}