{
  "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": "2026-04-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "Y",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "PTC",
      "openfda": {
        "k_number": [
          "K181675",
          "K242209",
          "K160990"
        ],
        "registration_number": [
          "3004193489",
          "1219029",
          "9616936",
          "3004145393",
          "3011979858"
        ],
        "fei_number": [
          "3002671736",
          "3004193489",
          "1219029",
          "3004145393",
          "3011979858"
        ]
      },
      "review_panel": "CH",
      "medical_specialty": "CH",
      "device_name": "Uric Acid Test System For At Home Prescription Use",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Clinical Chemistry",
      "device_class": "1",
      "definition": "For the quantitative measurement of uric acid in home use settings by patients diagnosed with gout. This device is for prescription use only.",
      "regulation_number": "862.1775",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}