X402 · Fda 510k

Search FDA 510(k) clearances by device name or applicant (manufacturer). Returns K-number, decision date, product code, decision description, and link to FDA summary. Pay 0.001 USDC on Base.

price

0.0010 USDC

rail

Base

facilitator

OMNIGATE

method

GET

endpoint https://mcp-x402.onrender.com/x402/fda-510k

payTo 0x5bbd32e0478e49a7540ef2d760e0b0f9aa6328b2

asset 0x833589fCD6eDb6E08f4c7C32D4f71b54bdA02913

indexed 2026-10-25T20:10:49.000Z

Live 402 challenge

Hits the real endpoint without paying and shows exactly what it demands. Nothing is charged.

Pay from your agent

import { wrapFetchWithPayment } from "@x402/fetch";
import { ExactEvmScheme } from "@x402/evm";
import { privateKeyToAccount } from "viem/accounts";

const signer = privateKeyToAccount(process.env.BUYER_PRIVATE_KEY);
const pay = wrapFetchWithPayment(fetch, { schemes: [{ network: "eip155:8453", client: new ExactEvmScheme(signer) }] });

const res = await pay("https://mcp-x402.onrender.com/x402/fda-510k", { method: "GET" });
console.log(await res.json(), res.headers.get("PAYMENT-RESPONSE"));

Example input

{
  "device": "pulse oximeter",
  "applicant": "Medtronic",
  "limit": 10
}

Example output

{
  "source": "openFDA device/510k",
  "query": {
    "device": "oximeter",
    "applicant": null,
    "search": "device_name:oximeter"
  },
  "total_found": 434,
  "returned": 10,
  "clearances": [
    {
      "k_number": "K252655",
      "device_name": "Pulse Oximeter (PO-A2AO, PO-A2AT, PO-A3AO, PO-H1AO, PO-B1AO, PO-C5AO, PO-C5AT, P",
      "applicant": "Shenzhen Imdk Medical Technology Co., Ltd.",
      "decision_date": "2026-05-11",
      "decision": "Substantially Equivalent",
      "product_code": "DQA",
      "summary_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252655"
    },
    {
      "k_number": "K252448",
      "device_name": "AViTA Pulse Oximeter (SP61)",
      "applicant": "Avita Corporation",
      "decision_date": "2026-02-27",
      "decision": "Substantially Equivalent",
      "product_code": "DQA",
      "summary_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252448"
    }
  ],
  "_disclaimer": "510(k) clearance means FDA found substantial equivalence to a predicate device —"
}