{
  "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": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "QWH",
      "openfda": {
        "k_number": [
          "K241453",
          "DEN220027"
        ],
        "registration_number": [
          "9610126",
          "3003561301",
          "3005847079"
        ],
        "fei_number": [
          "3002806559",
          "3003561301",
          "3005847079"
        ]
      },
      "review_panel": "TX",
      "medical_specialty": "CH",
      "device_name": "Prognostic Test For Development Or Progression Of Preeclampsia",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Clinical Chemistry",
      "device_class": "2",
      "definition": "A prognostic test for development or progression of preeclampsia is an in vitro diagnostic device intended to measure one or more analytes obtained from human samples. A prognostic test for development or progression of preeclampsia is indicated as an aid in the risk assessment for the development or progression of preeclampsia. This device is not intended for diagnosis of any disease.",
      "regulation_number": "862.1602",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}