{
  "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": "2026-10-26",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 15
    }
  },
  "results": [
    {
      "proprietary_name": [
        "QUIK-COMBO RTS pacing/defibrillation/ECG electrodes",
        "QUIK-COMBO pacing/defibrillation/ECG electrodes with REDI-PAK preconnected system",
        "QUIK-COMBO RTS Pediatric pacing/defibrillation/ECG electrodes",
        "QUIK-COMBO pacing/defibrillation/ECG electrodes"
      ],
      "establishment_type": [
        "Develop Specifications But Do Not Manufacture At This Facility"
      ],
      "registration": {
        "registration_number": "3015876",
        "fei_number": "3015876",
        "status_code": "1",
        "initial_importer_flag": "Y",
        "reg_expiry_date_year": "2027",
        "name": "PHYSIO-CONTROL, INC.",
        "address_line_1": "11811 WILLOWS RD., N.E.",
        "address_line_2": "",
        "city": "Redmond",
        "state_code": "WA",
        "iso_country_code": "US",
        "zip_code": "98052",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "STRYKER CORP.",
          "owner_operator_number": "1811755",
          "official_correspondent": {},
          "contact_address": {
            "address_1": "4100 East Milham Ave.",
            "address_2": "",
            "city": "Kalamazoo",
            "state_code": "MI",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "49001"
          }
        }
      },
      "pma_number": "P190007",
      "k_number": "",
      "products": [
        {
          "product_code": "MKJ",
          "created_date": "2020-12-08",
          "owner_operator_number": "1811755",
          "exempt": "",
          "openfda": {
            "device_name": "Automated External Defibrillators (Non-Wearable)",
            "medical_specialty_description": "Cardiovascular",
            "regulation_number": "870.5310",
            "device_class": "3"
          }
        }
      ]
    }
  ]
}