{
  "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": "2026-07-20",
    "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": "QAZ",
      "openfda": {
        "k_number": [
          "K182784",
          "K223597",
          "K211499",
          "DEN170046"
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        "registration_number": [
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        "fei_number": [
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      "review_panel": "PA",
      "medical_specialty": "MG",
      "device_name": "Cancer Predisposition Risk Assessment System",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Medical Genetics",
      "device_class": "2",
      "definition": "A qualitative in vitro molecular diagnostic system used for the detection of select variants in specified cancer-related genes. The device is intended to be used on genomic DNA isolated from human specimens collected by the user. The results of the test provide users with a genetic health risk assessment for developing certain cancers. The test may not include all variants associated with a predisposition of developing cancer and is not intended to describe a person’s overall risk of developing any type of cancer nor to aid in determination of treatment or act as a substitute for recommended cancer screenings or appropriate follow-up. The device is for over-the-counter use.",
      "regulation_number": "866.6090",
      "implant_flag": "N",
      "submission_type_id": "1"
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  ]
}