{
  "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": "2026-08-03",
    "results": {
      "skip": 0,
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    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "QQH",
      "openfda": {
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      "review_panel": "EN",
      "medical_specialty": "EN",
      "device_name": "Powered Insertion System For A Cochlear Implant Electrode Array",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Ear, Nose, Throat",
      "device_class": "2",
      "definition": "A powered insertion system for a cochlear implant electrode array is a prescription device used to assist in placing an electrode array into the cochlea.",
      "regulation_number": "874.4450",
      "implant_flag": "N",
      "submission_type_id": "1"
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}