{
  "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": 2
    }
  },
  "results": [
    {
      "proprietary_name": [
        "PEDIPLUS MANUAL RESUSCITATOR"
      ],
      "establishment_type": [
        "Manufacture Medical Device"
      ],
      "registration": {
        "registration_number": "3008818980",
        "fei_number": "3008818980",
        "status_code": "1",
        "initial_importer_flag": "Y",
        "reg_expiry_date_year": "2026",
        "name": "ICU Medical, Inc.",
        "address_line_1": "9124 Polk Lane, Suite 101",
        "address_line_2": "",
        "city": "Olive Branch",
        "state_code": "MS",
        "iso_country_code": "US",
        "zip_code": "38654",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "ICU Medical, Inc.",
          "owner_operator_number": "8020727",
          "official_correspondent": {
            "first_name": "Michelle",
            "middle_initial": "",
            "last_name": "Doherty",
            "subaccount_company_name": "",
            "phone_number": "x-949-3706562-x"
          },
          "contact_address": {
            "address_1": "951 Calle Amanecer",
            "address_2": "",
            "city": "San Clemente",
            "state_code": "CA",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "92673"
          }
        }
      },
      "pma_number": "",
      "k_number": "K023793",
      "products": [
        {
          "product_code": "BTM",
          "created_date": "2007-12-04",
          "owner_operator_number": "8020727",
          "exempt": "",
          "openfda": {
            "k_number": [
              "K023793"
            ],
            "device_name": "Ventilator, Emergency, Manual (Resuscitator)",
            "medical_specialty_description": "Anesthesiology",
            "regulation_number": "868.5915",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}