Device 510k

FDA 510(k) premarket clearances — the record of medical devices cleared for US marketing by demonstrating substantial equivalence to a predicate device.

Overview

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.

Endpoint

Method	Endpoint	Price	Description
GET	/v1/marketplace/api/device-510k	$0.00207	Invoke Device 510k (Search) and return the upstream response.

How to call it

Requests are paid per call over the x402 protocol. Call the endpoint, receive a 402 Payment Required quote, then repeat the request with the signed payment header. The SDKs do both steps for you.

# 1. Ask for a quote
curl -i https://api.jarvisclaw.ai/v1/marketplace/api/device-510k

# 2. Pay it (the SDK signs and retries for you)
curl -H "X-PAYMENT: <signed-payload>" https://api.jarvisclaw.ai/v1/marketplace/api/device-510k

Open in the marketplace