{
  "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": 4
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Venclose EVSRF Catheter; Venclose RF Ablation Catheter",
        "Venclose Foot Pedal",
        "Venclose System",
        "Venclose digiRF Generator",
        "Venclose Power Cord"
      ],
      "establishment_type": [
        "Manufacture Medical Device"
      ],
      "registration": {
        "registration_number": "3011879048",
        "fei_number": "3011879048",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2027",
        "name": "Venclose, Inc.",
        "address_line_1": "2570 N 1st St Fl 2 # 221",
        "address_line_2": "",
        "city": "San Jose",
        "state_code": "CA",
        "iso_country_code": "US",
        "zip_code": "95131",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "C.R. Bard",
          "owner_operator_number": "10049916",
          "official_correspondent": {
            "first_name": "Kristen",
            "middle_initial": "",
            "last_name": "Ortiz",
            "subaccount_company_name": "",
            "phone_number": "1-602-8305652-x"
          },
          "contact_address": {
            "address_1": "850 W Rio Salado Parkway",
            "address_2": "",
            "city": "Tempe",
            "state_code": "AZ",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "85281"
          }
        }
      },
      "pma_number": "",
      "k_number": "K160754",
      "products": [
        {
          "product_code": "GEI",
          "created_date": "2016-10-10",
          "owner_operator_number": "10049916",
          "exempt": "",
          "openfda": {
            "device_name": "Electrosurgical, Cutting & Coagulation & Accessories",
            "medical_specialty_description": "General, Plastic Surgery",
            "regulation_number": "878.4400",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}