{
  "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": "2026-06-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Eligible",
      "product_code": "OIH",
      "openfda": {
        "k_number": [
          "K131729"
        ]
      },
      "review_panel": "MI",
      "medical_specialty": "",
      "device_name": "Yersinia Spp. Reagents",
      "review_code": "",
      "unclassified_reason": "1",
      "medical_specialty_description": "Unknown",
      "device_class": "U",
      "definition": "Yersinia spp. reagents are devices that consist of Serological Reagents and Nucleic Acid Amplification Reagents to differentiate Yersinia spp. and presumptively identify Yersinia pestis (Y. pestis) from cultured isolates or clinical specimens.  They are indicated for use as an aid in the laboratory of diagnosis of plague.",
      "regulation_number": "",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}