{
  "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": {
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      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Eligible",
      "product_code": "OQU",
      "openfda": {
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      "review_panel": "AN",
      "medical_specialty": "AN",
      "device_name": "Airway Monitoring System",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Anesthesiology",
      "device_class": "2",
      "definition": "The device is intended to assist in verifying ett tube placement, assist in detecting ett tube movement and obstruction of the tube tip",
      "regulation_number": "868.5730",
      "implant_flag": "N",
      "submission_type_id": "1"
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}