{
  "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": "2026-07-20",
    "results": {
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Cambridge",
      "advisory_committee_description": "Ophthalmic",
      "address_1": "955 Massachusetts Ave. #335",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "QQU",
      "openfda": {
        "device_name": "Digital Therapy Device For Amblyopia",
        "medical_specialty_description": "Ophthalmic",
        "regulation_number": "886.5500",
        "device_class": "2",
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      "zip_code": "02139",
      "applicant": "Luminopia, Inc.",
      "decision_date": "2022-11-04",
      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "Luminopia One",
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      "contact": "Scott  Xiao",
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      "k_number": "K221659",
      "state": "MA",
      "date_received": "2022-06-08",
      "review_advisory_committee": "OP",
      "postal_code": "02139",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
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}