{
  "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": "NQM",
      "openfda": {
        "k_number": [
          "K110605",
          "K081767"
        ],
        "registration_number": [
          "2032098",
          "1720929",
          "1122236",
          "1722684",
          "1122376"
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        "fei_number": [
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          "3003572099",
          "1000220650",
          "3003058448"
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      },
      "review_panel": "CH",
      "medical_specialty": "CH",
      "device_name": "Immunoassay For Detection Of Amniotic Fluid Protein(S).",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Clinical Chemistry",
      "device_class": "1",
      "definition": "The test is for use by health care professionals to aid in the detection of fetal membrane rupture in pregnant women, when they report signs, symptoms or complaints suggestive of such rupture.",
      "regulation_number": "862.1550",
      "implant_flag": "N",
      "submission_type_id": "4"
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  ]
}