{
  "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": "2026-11-02",
    "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": "QTK",
      "openfda": {
        "registration_number": [
          "3014498720",
          "3013858269"
        ],
        "fei_number": [
          "3014498720",
          "3013858269"
        ]
      },
      "review_panel": "NE",
      "medical_specialty": "",
      "device_name": "Temporary Percutaneous Transluminal Cerebral Artery Dilatation Device",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Unknown",
      "device_class": "f",
      "definition": "Used to temporarily dilate and increase the diameter of cerebral arteries experiencing symptomatic vasospasm",
      "regulation_number": "",
      "implant_flag": "N",
      "submission_type_id": "6"
    }
  ]
}