{
  "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": "2026-08-03",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 57
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Inquiry AFocus II Diagnostic Catheter",
        "Inquiry Cardioversion Fixed Curve Diagnostic Catheter",
        "Inquiry Luma-Cath Fixed Curve Diagnostic Catheter",
        "Inquiry Luma-Cath Steerable Diagnostic Catheter",
        "Inquiry Steerable Diagnostic Catheter",
        "Inquiry Optima Diagnostic Catheter",
        "Inquiry Fixed Curve Diagnostic Catheter",
        "Response Electrophysiology Catheter",
        "Supreme Electrophysiology Catheter"
      ],
      "establishment_type": [
        "Manufacture Device in the United States for Export Only"
      ],
      "registration": {
        "registration_number": "2182269",
        "fei_number": "2182269",
        "status_code": "1",
        "initial_importer_flag": "Y",
        "reg_expiry_date_year": "2026",
        "name": "St. Jude Medical, Atrial Fibrillation Division, Inc.",
        "address_line_1": "14901 DEVEAU PL.",
        "address_line_2": "",
        "city": "Minnetonka",
        "state_code": "MN",
        "iso_country_code": "US",
        "zip_code": "55345",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "ABBOTT LABORATORIES",
          "owner_operator_number": "1415939",
          "official_correspondent": {},
          "contact_address": {
            "address_1": "100 ABBOTT PARK RD.",
            "address_2": "D-03Q3, AP52-1",
            "city": "Abbott Park",
            "state_code": "IL",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "60064"
          }
        }
      },
      "pma_number": "",
      "k_number": "",
      "products": [
        {
          "product_code": "DRF",
          "created_date": "2020-03-24",
          "owner_operator_number": "1415939",
          "exempt": "",
          "openfda": {
            "device_name": "Catheter, Electrode Recording, Or Probe, Electrode Recording",
            "medical_specialty_description": "Cardiovascular",
            "regulation_number": "870.1220",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}