{
  "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": {
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Metuchen",
      "advisory_committee_description": "Hematology",
      "address_1": "14 Michael Dr.",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "JBP",
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        "device_name": "Activated Whole Blood Clotting Time",
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        "regulation_number": "864.7140",
        "device_class": "2"
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      "zip_code": "08840",
      "applicant": "B & D Corp.",
      "decision_date": "1997-10-01",
      "decision_code": "SESE",
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      "device_name": "B&D ACTIVATED CLOTTING TIME (ACT) TEST TUBES BD-C101 (DIATOMACEOUS EARTH) AND BD-K101 (KAOLIN)",
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      "postal_code": "08840",
      "decision_description": "Substantially Equivalent",
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}