FDA 510(k) premarket clearances - the record of medical...
FDA 510(k) premarket clearances — the record of medical devices cleared for US marketing by demonstrating substantial equivalence to a predicate device. Search by device name, applicant (manufacturer), or FDA product code, and get back each clearance with its K-number, device name, applicant, decision date and decision description, clearance type (traditional/special/abbreviated), product code, advisory committee, and date received — newest decision first. Free, public-domain US government data. Authoritative regulatory-status data for medical-device diligence; point-in-time public records, not regulatory advice.
Request
- Base URL: https://2s.io
- URL: https://2s.io/api/medical/device-510k
- Auth: API key in header PAYMENT-SIGNATURE
Query parameters
Device.
Applicant.
Product code.
Maximum number of results to return.
Try before you buy. Set to 1 for one free real call per endpoint per hour — no wallet or payment needed — to verify the endpoint before paying. Equivalent to sending the "X-2s-Trial: 1" request header. Listed only on operations that offer a trial; the others always answer 402.
Response
Changes
No recorded changes to this operation across all 1 revision of this API.