{
  "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": "2026-08-03",
    "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": "QMV",
      "openfda": {
        "k_number": [
          "K220870",
          "K243463",
          "DEN200043"
        ],
        "registration_number": [
          "3002773840",
          "3010770794"
        ],
        "fei_number": [
          "3002773840",
          "3010770794"
        ]
      },
      "review_panel": "MI",
      "medical_specialty": "MI",
      "device_name": "Device To Detect And Identify Selected Microbial Agents That Cause Acute Febrile Illness",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Microbiology",
      "device_class": "2",
      "definition": "A device to detect and identify selected microbial agents that cause acute febrile illness is identified as a in vitro device intended for the detection and identification of microbial agents in human clinical specimens from patients with signs and symptoms of acute febrile illness who are at risk for exposure or who may have been exposed to these agents. It is intended to aid in the diagnosis of acute febrile illness in conjunction with other clinical, epidemiologic, and laboratory data, including patient travel, pathogen endemicity, or other risk factors.",
      "regulation_number": "866.3966",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}