{
  "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": "2026-11-02",
    "results": {
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  "results": [
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      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Eligible",
      "product_code": "PBC",
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      "medical_specialty": "HE",
      "device_name": "Manual Blood Grouping And Antibody Test Systems",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Hematology",
      "device_class": "2",
      "definition": "A manual blood grouping and antibody test system is used to group red blood cells and to detect antibodies to blood group antigens.",
      "regulation_number": "864.9175",
      "implant_flag": "N",
      "submission_type_id": "1"
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}