{
  "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": 2
    }
  },
  "results": [
    {
      "proprietary_name": [
        "ViaCath",
        "AcQRate Dx Steerable Catheter"
      ],
      "establishment_type": [
        "Manufacture Medical Device"
      ],
      "registration": {
        "registration_number": "8043831",
        "fei_number": "3002808439",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2027",
        "name": "VASCOMED INST KATHETERTECHNOLOGIE",
        "address_line_1": "HERTZALLEE 1",
        "address_line_2": "",
        "city": "BINZEN Baden-Wurttemberg",
        "state_code": "",
        "iso_country_code": "DE",
        "zip_code": "",
        "postal_code": "D79589",
        "us_agent": {
          "name": "Jon Brumbaugh",
          "business_name": "BIOTRONIK, Inc.",
          "bus_phone_area_code": "503",
          "bus_phone_num": "9707014",
          "bus_phone_extn": "",
          "fax_area_code": "",
          "fax_num": "",
          "email_address": "jon.brumbaugh@biotronik.com",
          "address_line_1": "6024 Jean Rd",
          "address_line_2": "",
          "city": "Lake Grove",
          "state_code": "OR",
          "iso_country_code": "US",
          "zip_code": "97035",
          "postal_code": ""
        },
        "owner_operator": {
          "firm_name": "VascoMed GmbH",
          "owner_operator_number": "9004075",
          "official_correspondent": {},
          "contact_address": {
            "address_1": "6024 Jean Road",
            "address_2": "",
            "city": "Lake Oswego",
            "state_code": "OR",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "97035"
          }
        }
      },
      "pma_number": "",
      "k_number": "K212593",
      "products": [
        {
          "product_code": "DRF",
          "created_date": "2021-10-20",
          "owner_operator_number": "9004075",
          "exempt": "",
          "openfda": {
            "k_number": [
              "K212593"
            ],
            "device_name": "Catheter, Electrode Recording, Or Probe, Electrode Recording",
            "medical_specialty_description": "Cardiovascular",
            "regulation_number": "870.1220",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}