{
  "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": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Somerset",
      "advisory_committee_description": "General, Plastic Surgery",
      "address_1": "200 Franklin Sq. Dr.",
      "address_2": "P.O. Box 6800",
      "statement_or_summary": "Summary",
      "product_code": "FTC",
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        "device_name": "Light, Ultraviolet, Dermatological",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4630",
        "device_class": "2"
      },
      "zip_code": "08875",
      "applicant": "Philips Lighting Co.",
      "decision_date": "2002-05-16",
      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "PHILIPS TL 20W/01RS UV-B, PHILIPS PL-S 9W/01/2P UV, AND PHILIPS PL-L 36W/01/4P UV-B",
      "advisory_committee": "SU",
      "contact": "TONI J HOFFMANN",
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      "k_number": "K021092",
      "state": "NJ",
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      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
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}