fda_device_510k

Active

Tool of io.github.blackboxfoundry/livedatalink

declared in 1.0.0

FDA 510(k) clearances for medical devices. The 510(k) pathway is how most non-high-risk devices come to market in the US. Filter by manufacturer (applicant), device name, product code, or decision date range. Used for competitive intel, device R&D scouting, M&A research.

Parameters schema

{
  "type": "object",
  "$schema": "http://json-schema.org/draft-07/schema#",
  "properties": {
    "limit": {
      "type": "number",
      "description": "Maximum rows to return (default 25, max 100)."
    },
    "query": {
      "type": "string",
      "description": "Manufacturer (applicant) name or device name search term."
    },
    "end_date": {
      "type": "string",
      "description": "Inclusive ISO date upper bound (YYYY-MM-DD)."
    },
    "start_date": {
      "type": "string",
      "description": "Inclusive ISO date lower bound (YYYY-MM-DD)."
    },
    "product_code": {
      "type": "string",
      "description": "Optional product code (e.g. 'DXJ' for ECG)."
    }
  },
  "additionalProperties": false
}

What this tool wraps· 0 endpoints

min confidence0.70 0.50

No endpoints wrapped at confidence ≥ 0.50.

Parent server

io.github.blackboxfoundry/livedatalink

https://github.com/blackboxfoundry/livedatalink

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