{
  "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": "2026-07-27",
    "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": "NRK",
      "openfda": {
        "registration_number": [
          "3042617034",
          "3015259871",
          "3027256314",
          "3022472576",
          "3042838444",
          "3007972833",
          "3017503380"
        ],
        "fei_number": [
          "3042617034",
          "3015259871",
          "3027256314",
          "3022472576",
          "3042838444",
          "3007972833",
          "3017503380"
        ],
        "k_number": [
          "DEN050007"
        ]
      },
      "review_panel": "EN",
      "medical_specialty": "EN",
      "device_name": "Kit, Test, Olfactory",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Ear, Nose, Throat",
      "device_class": "2",
      "definition": "The home test for loss of the sense of smell is packaged in a small carton which contains (1) an instruction book, (2) a booklet containing twelve micorencapsulated smell strips, each on a separate page, with instructions for scoring the test and an answer key, and (3) a physician information card.  The device is intended for screening neurological disorder.",
      "regulation_number": "874.1600",
      "implant_flag": "N",
      "submission_type_id": "4"
    }
  ]
}