{
  "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": "2026-05-25",
    "results": {
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Suzhou",
      "advisory_committee_description": "Radiology",
      "address_1": "Rm. 3a05, Bldg. 2, #8 Changting Rd., High-Tech Zone",
      "address_2": "",
      "statement_or_summary": "Summary",
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      "applicant": "Compai Healthcare (Suzhou) Co.,Ltd",
      "decision_date": "2023-04-24",
      "decision_code": "SESE",
      "country_code": "CN",
      "device_name": "TrueView 200 Pro-US Specimen Radiography System (TrueView 200 Pro-US)",
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      "date_received": "2023-01-18",
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      "decision_description": "Substantially Equivalent",
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}