{
  "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": "Frederick",
      "advisory_committee_description": "Physical Medicine",
      "address_1": "4539 Metropolitan Ct.",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "PQY",
      "openfda": {
        "device_name": "Nonthermal Shortwave Therapy Device Indicated For Over The Counter Use For The Treatment Of Pain",
        "medical_specialty_description": "Physical Medicine",
        "regulation_number": "890.5290",
        "device_class": "2",
        "registration_number": [
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          "3007282994",
          "9611956",
          "3004837702"
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          "1511629",
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          "3005550216"
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      "zip_code": "21704",
      "applicant": "Bioelectronics Corporation",
      "decision_date": "2020-01-31",
      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "ActiPatch",
      "advisory_committee": "PM",
      "contact": "Sree N. Koneru",
      "expedited_review_flag": "",
      "k_number": "K192234",
      "state": "MD",
      "date_received": "2019-08-19",
      "review_advisory_committee": "PM",
      "postal_code": "21704",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
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  ]
}