{
  "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": "2026-06-01",
    "results": {
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      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "QBR",
      "openfda": {
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      "review_panel": "OP",
      "medical_specialty": "OP",
      "device_name": "Intranasal Electrostimulation Device For Dry Eye Symptoms",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Ophthalmic",
      "device_class": "2",
      "definition": "This device type is intended to temporarily increase tear production using neurostimulation to improve dry eye symptoms. For prescription use only.",
      "regulation_number": "886.5310",
      "implant_flag": "N",
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}