{
  "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,
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      "third_party_flag": "N",
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      "summary_malfunction_reporting": "Eligible",
      "product_code": "PZF",
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      "device_name": "Mers-Cov And Common Respiratory Pathogens Multiplex Nucleic Acid Detection System",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Pathology",
      "device_class": "2",
      "definition": "A Middle East Respiratory Syndrome Coronavirus (MERS-CoV) and common respiratory pathogens multiplex nucleic acid detection system is a qualitative in vitro diagnostic test for the detection and identification of MERS-CoV and common respiratory pathogens – associated nucleic acids in human clinical specimens. The test is indicated for individuals meeting specific MERS-CoV clinical and/or epidemiological criteria. It aids in the differential diagnosis of MERS-CoV infection in conjunction with other clinical, epidemiologic, and laboratory data, in accordance with the guidelines provided by the appropriate public health authorities.",
      "regulation_number": "866.4001",
      "implant_flag": "N",
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}