{
  "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",
      "city": "Hopkins",
      "advisory_committee_description": "Neurology",
      "address_1": "153 Ashley Rd.",
      "address_2": "",
      "statement_or_summary": "",
      "product_code": "QMZ",
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        "device_name": "Digital Therapy Device To Reduce Sleep Disturbance For Psychiatric Conditions",
        "medical_specialty_description": "Neurology",
        "regulation_number": "882.5705",
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      "zip_code": "55343",
      "applicant": "Nightware, Inc.",
      "decision_date": "2020-11-06",
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      "country_code": "US",
      "device_name": "NightWare Kit, Apple iPhone, Apple Watch, Apple iPhone Charging Cable, Apple Watch Charging Cable",
      "advisory_committee": "NE",
      "contact": "Grady  Hannah",
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      "k_number": "DEN200033",
      "state": "MN",
      "date_received": "2020-05-27",
      "review_advisory_committee": "NE",
      "postal_code": "55343",
      "decision_description": "Unknown",
      "clearance_type": "Direct"
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}