{
  "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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    {
      "third_party_flag": "N",
      "city": "Washington",
      "advisory_committee_description": "Physical Medicine",
      "address_1": "1220 19th St., NW",
      "address_2": "Suite 300",
      "statement_or_summary": "Summary",
      "product_code": "ILX",
      "openfda": {
        "device_name": "Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat",
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        "regulation_number": "890.5290",
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      "applicant": "Promedtek, Inc.",
      "decision_date": "2007-05-24",
      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "MODEL PMT850",
      "advisory_committee": "PM",
      "contact": "DIANE  MANDELL",
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      "k_number": "K070931",
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      "decision_description": "Substantially Equivalent",
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