{
  "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": "2026-07-27",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "QTE",
      "openfda": {
        "k_number": [
          "K202852"
        ],
        "registration_number": [
          "3008629194"
        ],
        "fei_number": [
          "3008629194"
        ]
      },
      "review_panel": "IM",
      "medical_specialty": "IM",
      "device_name": "Thymidine Kinase Activity",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Immunology",
      "device_class": "2",
      "definition": "In vitro test to measure thymidine kinase activity (TKa) to aid in monitoring disease progression of breast cancer patients.",
      "regulation_number": "866.6010",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}