{
  "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": "SEF",
      "openfda": {
        "k_number": [
          "K242429"
        ],
        "registration_number": [
          "3006260740",
          "9617592",
          "3015924373"
        ],
        "fei_number": [
          "3006260740",
          "3002468371",
          "3015924373"
        ]
      },
      "review_panel": "HO",
      "medical_specialty": "HO",
      "device_name": "Central Venous Catheter With Manual Insertion System",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "General Hospital",
      "device_class": "2",
      "definition": "A central venous catheter with manual insertion system is intended to provide short-term access (<30 days) to the central venous system. The manual insertion system is attached to the catheter and facilitates placement in the targeted vessel.",
      "regulation_number": "880.5200",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}