{
  "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": "QVB",
      "openfda": {
        "k_number": [
          "K252306",
          "K251559",
          "DEN220042"
        ],
        "registration_number": [
          "3015392401",
          "3013145340"
        ],
        "fei_number": [
          "3015392401",
          "3013145340"
        ]
      },
      "review_panel": "HO",
      "medical_specialty": "HO",
      "device_name": "Biological Sterilization Indicator With Indirect Growth Detection",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "General Hospital",
      "device_class": "2",
      "definition": "A biological sterilization indicator with indirect growth detection capabilities is a device intended for use by a healthcare provider to accompany products being sterilized through a sterilization process to monitor the adequacy of sterilization. Detection of surviving microorganisms is accomplished by a method other than direct detection of growth or growth products.",
      "regulation_number": "880.2806",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}