{
  "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",
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      "summary_malfunction_reporting": "Eligible",
      "product_code": "PLZ",
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      "review_panel": "OP",
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      "device_name": "Ocular Pattern Recorder",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Ophthalmic",
      "device_class": "2",
      "definition": "A diurnal pattern recorder system is a non-implantable, prescription device incorporating a telemetric sensor intended to detect changes in ocular dimension for monitoring diurnal patterns of IOP fluctuation.",
      "regulation_number": "886.1925",
      "implant_flag": "N",
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}