{
  "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": "2026-06-01",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "city": "Shenzhen",
      "advisory_committee_description": "Obstetrics/Gynecology",
      "address_1": "Rm. 20203, Bldg. 6, Donglongxing Kejiyuan, Huaning Rd.",
      "address_2": "Xinshishequ, Dalang St.",
      "statement_or_summary": "Summary",
      "product_code": "KNG",
      "openfda": {
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        "device_name": "Monitor, Ultrasonic, Fetal",
        "medical_specialty_description": "Obstetrics/Gynecology",
        "regulation_number": "884.2660",
        "device_class": "2"
      },
      "zip_code": "518109",
      "applicant": "Shenzhen Mericonn Technology Co., Ltd.",
      "decision_date": "2021-11-03",
      "decision_code": "SESE",
      "country_code": "CN",
      "device_name": "Fetal Doppler",
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      "contact": "Jiang  Chuanyuan",
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      "k_number": "K212084",
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      "date_received": "2021-07-02",
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      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
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}