{
  "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",
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    {
      "third_party_flag": "N",
      "city": "Suzhou",
      "advisory_committee_description": "General, Plastic Surgery",
      "address_1": "101 Rm., B8 Bldg., 218 Xinghu St.,",
      "address_2": "Suzhou Industrial Park",
      "statement_or_summary": "Summary",
      "product_code": "QAU",
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        "device_name": "Hemostatic Device For Endoscopic Gastrointestinal Use",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4456",
        "device_class": "2"
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      "zip_code": "215000",
      "applicant": "Endoclot Plus Co., Ltd.",
      "decision_date": "2021-01-29",
      "decision_code": "SESE",
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      "contact": "Huihui  Xie",
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      "k_number": "K190677",
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      "date_received": "2019-03-15",
      "review_advisory_committee": "SU",
      "postal_code": "215000",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
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}