{
  "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": "ODF",
      "openfda": {
        "k_number": [
          "K912089",
          "K091962",
          "K052194",
          "K963354",
          "K943593",
          "K090170",
          "K910732",
          "K941230",
          "K933106",
          "K050403",
          "K092739",
          "K874858"
        ],
        "registration_number": [
          "1225984"
        ],
        "fei_number": [
          "3002516162"
        ]
      },
      "review_panel": "GU",
      "medical_specialty": "GU",
      "device_name": "Mini Endoscope, Gastroenterology-Urology",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Gastroenterology, Urology",
      "device_class": "2",
      "definition": "To examine and perform procedures in body cavities of the GI and GU tract.    If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).",
      "regulation_number": "876.1500",
      "implant_flag": "N",
      "submission_type_id": "1"
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}