{
  "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,
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  "results": [
    {
      "third_party_flag": "Y",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Eligible",
      "product_code": "POP",
      "openfda": {
        "k_number": [
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      "review_panel": "NE",
      "medical_specialty": "NE",
      "device_name": "Cranial Motion Measurement Device",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Neurology",
      "device_class": "2",
      "definition": "A cranial motion measurement device is a prescription device that utilizes accelerometers to measure the motion or acceleration of the skull.  These measurements are not to be used for diagnostic purposes.",
      "regulation_number": "882.1630",
      "implant_flag": "N",
      "submission_type_id": "1"
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  ]
}