{
  "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": "2026-04-13",
    "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": "OPP",
      "openfda": {
        "k_number": [
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          "K252757",
          "K093065",
          "K100947",
          "K163357",
          "K111924",
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        ],
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      "review_panel": "CH",
      "medical_specialty": "HO",
      "device_name": "Pump, Infusion, Insulin Bolus",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "General Hospital",
      "device_class": "2",
      "definition": "The device is adhered to the body for several days for the purpose of periodically infusing an insulin bolus.",
      "regulation_number": "880.5725",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
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}