{
  "x402Version": 2,
  "id": 14578,
  "slug": "14578",
  "resource": "https://api.govparse.io/v1/fda/device-clearances/search",
  "description": "Which companies just cleared or got FDA approval for a medical device? Search openFDA device 510(k) clearances and PMA premarket approvals by applicant company, pathway (510k/pma), FDA product code, advisory-committee specialty (e.g. Cardiovascular), applicant state, or decision date (since). Returns the applicant company (entity-resolved where possible), device name, product code, and decision date — a fresh target list for device and component sellers. openFDA public-domain records.",
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  "outputSchema": {
    "bazaar": {
      "info": {
        "input": {
          "method": "GET",
          "queryParams": {
            "company": "Medtronic",
            "pathway": "510k",
            "product_code": "DXY"
          },
          "type": "http"
        },
        "output": {
          "example": {
            "rows": [
              {
                "advisory_committee": "Cardiovascular",
                "applicant": "Pacesetter Systems",
                "clearance_type": "Traditional",
                "date_received": "1985-02-19",
                "decision_code": "SESE",
                "decision_date": "1985-04-01",
                "decision_description": "Substantially Equivalent",
                "decision_id": "K850651",
                "device_name": "PROGRAMALITH III-3 MODEL 231 PULSE GENERATOR",
                "entity_id": null,
                "generic_name": null,
                "pathway": "510k",
                "product_code": "DXY",
                "state": "CA"
              }
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            "total_matched": 1
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          "type": "json"
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      "routeTemplate": "/v1/fda/device-clearances/search",
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          "input": {
            "properties": {
              "advisory_committee": {
                "description": "Medical specialty panel fragment.",
                "examples": [
                  "Cardiovascular"
                ],
                "type": "string"
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              "company": {
                "description": "Applicant company — suffix/punctuation-insensitive.",
                "examples": [
                  "Medtronic"
                ],
                "type": "string"
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              "entity_id": {
                "description": "Resolved employer entity UUID.",
                "examples": [
                  "b7f3e2d1-4a5c-4e6f-8a9b-0c1d2e3f4a5b"
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              "offset": {
                "description": "Rows to skip.",
                "examples": [
                  0
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                "type": "integer"
              },
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                "examples": [
                  "510k"
                ],
                "type": "string"
              },
              "product_code": {
                "description": "FDA product code(s), CSV.",
                "examples": [
                  "DXY"
                ],
                "type": "string"
              },
              "since": {
                "description": "Decision (clearance/approval) date on/after this date (YYYY-MM-DD).",
                "examples": [
                  "2026-01-01"
                ],
                "type": "string"
              },
              "sort": {
                "description": "decision_date | date_received :asc|:desc. Default decision_date:desc.",
                "examples": [
                  "decision_date:desc"
                ],
                "type": "string"
              },
              "state": {
                "description": "Applicant state code(s), CSV (510(k) only).",
                "examples": [
                  "CA"
                ],
                "type": "string"
              }
            },
            "required": [],
            "type": "object"
          }
        },
        "type": "object"
      }
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  "featured": false,
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    "submitted_at": "2026-09-18T22:00:31.484Z"
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}