{
  "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": 95
    }
  },
  "results": [
    {
      "proprietary_name": [
        "4F Infiniti Diagnostic Catheter",
        "4F & 5F Nylex Diagnostic Catheters",
        "4F & 5F Tempo Diagnostic Catheters"
      ],
      "establishment_type": [
        "Develop Specifications But Do Not Manufacture At This Facility",
        "Complaint File Establishment per 21 CFR 820.198"
      ],
      "registration": {
        "registration_number": "1016427",
        "fei_number": "1016427",
        "status_code": "1",
        "initial_importer_flag": "Y",
        "reg_expiry_date_year": "2026",
        "name": "Cordis US Corp.",
        "address_line_1": "14201 N.W. 60TH AVE.",
        "address_line_2": "",
        "city": "Miami Lakes",
        "state_code": "FL",
        "iso_country_code": "US",
        "zip_code": "33014",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Cordis US Corp.",
          "owner_operator_number": "1016427",
          "official_correspondent": {
            "first_name": "Linda",
            "middle_initial": "",
            "last_name": "Ruedy",
            "subaccount_company_name": "",
            "phone_number": "1-408-2733423-x"
          },
          "contact_address": {
            "address_1": "5452 Betsy Ross Drive",
            "address_2": "--",
            "city": "Santa Clara",
            "state_code": "CA",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "95054"
          }
        }
      },
      "pma_number": "",
      "k_number": "K181836",
      "products": [
        {
          "product_code": "DQO",
          "created_date": "2022-06-15",
          "owner_operator_number": "1016427",
          "exempt": "",
          "openfda": {
            "device_name": "Catheter, Intravascular, Diagnostic",
            "medical_specialty_description": "Cardiovascular",
            "regulation_number": "870.1200",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}