{
  "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": "2026-06-01",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "NUI",
      "openfda": {
        "k_number": [
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      "review_panel": "NE",
      "medical_specialty": "CV",
      "device_name": "Ultrasound, Infusion, System",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Cardiovascular",
      "device_class": "2",
      "definition": "For regional infusion of contrast materials into selected vessels in the neuro-vasculature.  The device may be used for controlled, regional infusion into selected vessels and is not intended for use in the coronary vasculature.",
      "regulation_number": "870.1200",
      "implant_flag": "N",
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}