{
  "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": "QUD",
      "openfda": {
        "k_number": [
          "DEN220065"
        ],
        "registration_number": [
          "3027502350",
          "3007766601",
          "3005580113"
        ],
        "fei_number": [
          "3027502350",
          "3007766601",
          "3005580113"
        ]
      },
      "review_panel": "GU",
      "medical_specialty": "GU",
      "device_name": "Blood Detection Capsule",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Gastroenterology, Urology",
      "device_class": "2",
      "definition": "Ingestible gastrointestinal blood detection capsule device is a prescription device that uses spectrophotometry (light absorption technology) to detect the presence or absence of blood in the gastrointestinal tract.",
      "regulation_number": "876.1390",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}