{
  "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": "ODY",
      "openfda": {
        "k_number": [
          "K063048",
          "K122263"
        ],
        "registration_number": [
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          "1721504",
          "3012536737",
          "1061124",
          "3015225571",
          "3033589330",
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      },
      "review_panel": "HO",
      "medical_specialty": "HO",
      "device_name": "Tunneled Catheter Remover",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "General Hospital",
      "device_class": "2",
      "definition": "To assist in the removal of tunneled long term catheter cuffs using a minimal invasive technique by seperating the tissue ingrowth cuff from the surrounding tissue. Following seperation of the cuff from the tissue, the catheter can be safely removed from the body.",
      "regulation_number": "880.5970",
      "implant_flag": "N",
      "submission_type_id": "1"
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  ]
}