{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "QVJ",
      "openfda": {
        "k_number": [
          "K213247",
          "K223440",
          "K220493",
          "K233760"
        ],
        "registration_number": [
          "3022327202",
          "3013924508",
          "3013563737",
          "3017954802",
          "3038715747"
        ],
        "fei_number": [
          "3022327202",
          "3013924508",
          "3013563737",
          "3017954802",
          "3038715747"
        ]
      },
      "review_panel": "SU",
      "medical_specialty": "SU",
      "device_name": "Low Power Electrosurgical Devices For Skin Lesion Destruction",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "General, Plastic Surgery",
      "device_class": "2",
      "definition": "For the removal and destruction of skin lesions in general dermatological procedures, also referred to as Plasma Pen Devices, which  generates electrical arc in the ambient air between an electrical probe tip and the skin and cause intended tissue damage for the removal and destruction of skin lesions",
      "regulation_number": "878.4400",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}