{
  "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": "2026-08-31",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Beijing",
      "advisory_committee_description": "Obstetrics/Gynecology",
      "address_1": "Rm. 201 B2 Diamond Center, #66 Xixiaokou Rd.",
      "address_2": "Haidian District",
      "statement_or_summary": "Summary",
      "product_code": "MQL",
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        "medical_specialty_description": "Obstetrics/Gynecology",
        "regulation_number": "884.6180",
        "device_class": "2"
      },
      "zip_code": "100192",
      "applicant": "CELL STORE (BEIJING) BIOTECHNOLOGY CO., LTD.",
      "decision_date": "2026-08-28",
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      "country_code": "CN",
      "device_name": "Vitrification Freeze Kit and Thawing Kit (CS-IVF-FK; CS-IVF-TK)",
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      "date_received": "2025-12-30",
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      "decision_description": "Substantially Equivalent",
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}