{
  "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": "2026-07-27",
    "results": {
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Leesburg",
      "advisory_committee_description": "Physical Medicine",
      "address_1": "5818 Princess Caroline Pl.",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "NZY",
      "openfda": {
        "device_name": "Light, Lymphedema Reduction, Low Energy",
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      "applicant": "Riancorp Pty, Ltd.",
      "decision_date": "2004-12-23",
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      "device_name": "LTU-904 PORTABLE LASER THERAPY UNIT",
      "advisory_committee": "PM",
      "contact": "ROBERT T HANDREN",
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      "k_number": "K030295",
      "state": "FL",
      "date_received": "2003-01-28",
      "review_advisory_committee": "SU",
      "postal_code": "34748",
      "decision_description": "Substantially Equivalent",
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}