fda_device_510k
ActiveTool 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
}No endpoints wrapped at confidence ≥ 0.70.
Parent server
io.github.blackboxfoundry/livedatalink
https://github.com/blackboxfoundry/livedatalink
2/7 registries