{
  "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": "2026-07-20",
    "results": {
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Los Angeles",
      "advisory_committee_description": "General, Plastic Surgery",
      "address_1": "11661 San Vicente Blvd.",
      "address_2": "Suite 203",
      "statement_or_summary": "",
      "product_code": "LNK",
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        "device_name": "Laser For Gastro-Urology Use",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4810",
        "device_class": "2"
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      "zip_code": "90049",
      "applicant": "Directed Energy, Inc.",
      "decision_date": "1987-05-18",
      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "MODEL 20-C WITH AN SA-20A/U OPT. ATTACH. HEMORRHO.",
      "advisory_committee": "SU",
      "contact": "EDWARD  JOHANSEN",
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      "k_number": "K871032",
      "state": "CA",
      "date_received": "1987-03-16",
      "review_advisory_committee": "GU",
      "postal_code": "90049",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
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}