{
  "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": "2026-07-27",
    "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": "QNX",
      "openfda": {
        "k_number": [
          "DEN200017"
        ],
        "registration_number": [
          "3021373862",
          "3008972967"
        ],
        "fei_number": [
          "3021373862",
          "3008972967"
        ]
      },
      "review_panel": "PM",
      "medical_specialty": "NE",
      "device_name": "External Compression Device For Internal Jugular Vein Compression",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Neurology",
      "device_class": "2",
      "definition": "External compression device for internal jugular vein compression. An external compression device for internal jugular vein compression is a non-invasive device that is intended to increase intracranial blood volume to reduce the occurrence of specific changes in the brain following head impacts sustained from the environment of use.",
      "regulation_number": "890.3050",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}