{
  "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": "2026-09-14",
    "results": {
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Dongguan",
      "advisory_committee_description": "Dental",
      "address_1": "#13 Jingci Rd., Shilong",
      "address_2": "",
      "statement_or_summary": "Statement",
      "product_code": "SJH",
      "openfda": {},
      "zip_code": "523326",
      "applicant": "Lakong Medical Devices Co., Ltd.",
      "decision_date": "2026-09-10",
      "decision_code": "SESE",
      "country_code": "CN",
      "device_name": "Portable Dental Unit (PC 2630, OMC 2375CV, MC 3600CV)",
      "advisory_committee": "DE",
      "contact": "Zhongliang  Wang",
      "expedited_review_flag": "",
      "k_number": "K254009",
      "state": "",
      "date_received": "2025-12-15",
      "review_advisory_committee": "DE",
      "postal_code": "523326",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
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}