{
  "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": "NKI",
      "openfda": {
        "registration_number": [
          "3026042200",
          "3027475369"
        ],
        "fei_number": [
          "3026042200",
          "3027475369"
        ],
        "k_number": [
          "K033193"
        ]
      },
      "review_panel": "NE",
      "medical_specialty": "OR",
      "device_name": "Goniometer With Electrodes",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Orthopedic",
      "device_class": "2",
      "definition": "A goniometer is an AC-powered or battery powered  device intended to evaluate joint function by measuring and recording range of motion, acceleration, or forces exerted by a joint. The class II (special controls) goniometer uses transcutaneous adhesive electrode lead wires and patient cables to transmit and record patient data.",
      "regulation_number": "888.1500",
      "implant_flag": "N",
      "submission_type_id": "4"
    }
  ]
}