{
  "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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    {
      "third_party_flag": "N",
      "city": "Weihai",
      "advisory_committee_description": "Obstetrics/Gynecology",
      "address_1": "#1, Weigao Rd.",
      "address_2": "Torch High-Tech Industrial Development Zone",
      "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": "",
      "applicant": "Shandong Wego Ruisheng Medical Device Co., Ltd.",
      "decision_date": "2024-07-01",
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      "device_name": "Cryo-straw (Type I, Type III); Warming Kit (A-4ML, B-8ML); Vitrification Kit (A-3ML, B-6ML)",
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      "k_number": "K233477",
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      "date_received": "2023-10-26",
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      "postal_code": "",
      "decision_description": "Substantially Equivalent",
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}