{
  "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": 37
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Reprocessed Diagnostic Electrophysiology Catheter"
      ],
      "establishment_type": [
        "Reprocess Single-Use Device"
      ],
      "registration": {
        "registration_number": "3011610434",
        "fei_number": "3011610434",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2027",
        "name": "INNOVATIVE HEALTH, LLC.",
        "address_line_1": "1435 N. Hayden Road",
        "address_line_2": "Suite 100",
        "city": "Scottsdale",
        "state_code": "AZ",
        "iso_country_code": "US",
        "zip_code": "85257",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Innovative Health, LLC.",
          "owner_operator_number": "10048854",
          "official_correspondent": {
            "first_name": "Angelica",
            "middle_initial": "",
            "last_name": "McParlane",
            "subaccount_company_name": "",
            "phone_number": "1-877-4003740-x"
          },
          "contact_address": {
            "address_1": "1435 N. Hayden Road",
            "address_2": "Suite 100",
            "city": "Scottsdale",
            "state_code": "AZ",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "85257"
          }
        }
      },
      "pma_number": "",
      "k_number": "K161393",
      "products": [
        {
          "product_code": "NLH",
          "created_date": "2016-11-06",
          "owner_operator_number": "10048854",
          "exempt": "",
          "openfda": {
            "device_name": "Catheter, Recording, Electrode, Reprocessed",
            "medical_specialty_description": "Cardiovascular",
            "regulation_number": "870.1220",
            "device_class": "2"
          }
        },
        {
          "product_code": "DRF",
          "created_date": "2016-11-06",
          "owner_operator_number": "10048854",
          "exempt": "",
          "openfda": {
            "device_name": "Catheter, Electrode Recording, Or Probe, Electrode Recording",
            "medical_specialty_description": "Cardiovascular",
            "regulation_number": "870.1220",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}