{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-10-05",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "pma_number": "P030005",
      "supplement_number": "S252",
      "applicant": "Guidant Corp.",
      "street_1": "4100 Hamline Ave. N",
      "street_2": "",
      "city": "St Paul",
      "state": "MN",
      "zip": "55112",
      "zip_ext": "",
      "generic_name": "Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)",
      "trade_name": "CONTAK RENEWAL MODELS H125 AND H120 WITH THE MODEL 2865 VERSION 1.8 APPLICATION SOFTWARE",
      "product_code": "NKE",
      "advisory_committee": "CV",
      "advisory_committee_description": "Cardiovascular",
      "supplement_type": "30-Day Notice",
      "supplement_reason": "Process Change - Manufacturer/Sterilizer/Packager/Supplier",
      "expedited_review_flag": "N",
      "date_received": "2026-03-03",
      "decision_date": "2026-04-01",
      "docket_number": "",
      "decision_code": "OK30",
      "ao_statement": "",
      "openfda": {
        "registration_number": [
          "9610139",
          "2182208",
          "2124215",
          "3006705815",
          "2017865",
          "3008483389",
          "3009380063",
          "2649622",
          "1220452",
          "3003120897",
          "2135338",
          "2133641",
          "3033257494",
          "1028232",
          "3005334138",
          "3008494315",
          "3013500228",
          "9614453",
          "3012552532",
          "9616693",
          "3015453963",
          "2032521",
          "3013288201",
          "3013596024",
          "3018094310"
        ],
        "fei_number": [
          "2182208",
          "2124215",
          "3006705815",
          "2017865",
          "3008483389",
          "3009380063",
          "2649622",
          "1220452",
          "3000203466",
          "3003120897",
          "3002806500",
          "3033257494",
          "1028232",
          "3005334138",
          "3013500228",
          "3005700659",
          "3012552532",
          "3002618605",
          "3003574398",
          "3015453963",
          "3013288201",
          "3013596024",
          "3008377825",
          "3018094310",
          "3002807576"
        ],
        "device_name": "Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}