{
  "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": "2026-10-19",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 48
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Cough Assist"
      ],
      "establishment_type": [
        "Repack or Relabel Medical Device",
        "Complaint File Establishment per 21 CFR 820.198"
      ],
      "registration": {
        "registration_number": "3006446479",
        "fei_number": "3006446479",
        "status_code": "1",
        "initial_importer_flag": "Y",
        "reg_expiry_date_year": "2026",
        "name": "SUNSET HEALTHCARE SOLUTIONS, Inc.",
        "address_line_1": "141 W Jackson Blvd Ste 1950",
        "address_line_2": "",
        "city": "CHICAGO",
        "state_code": "IL",
        "iso_country_code": "US",
        "zip_code": "60604",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Sunset Healthcare Solutions",
          "owner_operator_number": "9106379",
          "official_correspondent": {
            "first_name": "JOSEPH",
            "middle_initial": "-",
            "last_name": "CONSOLI",
            "subaccount_company_name": "",
            "phone_number": "1-773-5190969-x"
          },
          "contact_address": {
            "address_1": "141 West Jackson Boulevard",
            "address_2": "1950",
            "city": "Chicago",
            "state_code": "IL",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "60604"
          }
        }
      },
      "pma_number": "",
      "k_number": "K121955",
      "products": [
        {
          "product_code": "NHJ",
          "created_date": "2026-08-13",
          "owner_operator_number": "9106379",
          "exempt": "",
          "openfda": {
            "device_name": "Device, Positive Pressure Breathing, Intermittent",
            "medical_specialty_description": "Anesthesiology",
            "regulation_number": "868.5905",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}