{
  "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": "2026-04-13",
    "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": "QRA",
      "openfda": {
        "k_number": [
          "K243417",
          "K251519",
          "DEN210014",
          "K230825",
          "K254004",
          "K230814"
        ],
        "registration_number": [
          "3042903607",
          "3021071568"
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        "fei_number": [
          "3042903607",
          "3021071568"
        ]
      },
      "review_panel": "PM",
      "medical_specialty": "NE",
      "device_name": "Virtual Reality Behavioral Therapy Device For Pain Relief",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Neurology",
      "device_class": "2",
      "definition": "A virtual reality behavioral therapy device for pain relief is a device intended to provide behavioral therapy for patients with pain. Therapy is administered via a virtual reality display which utilizes a software program containing the behavioral therapy content.",
      "regulation_number": "890.5800",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}