{
  "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": "2026-08-03",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "QIT",
      "openfda": {
        "pma_number": [
          "P180035"
        ],
        "registration_number": [
          "3003981983",
          "3002296055",
          "3005724763",
          "3008586477",
          "3030421258",
          "3011771819",
          "9614374"
        ],
        "fei_number": [
          "3003981983",
          "3002807783",
          "3002296055",
          "3005724763",
          "3008586477",
          "3030421258",
          "3011771819"
        ]
      },
      "review_panel": "OP",
      "medical_specialty": "",
      "device_name": "Daily Wear Soft Contact Lens To Reduce The Progression Of Myopia",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Unknown",
      "device_class": "3",
      "definition": "Intended to be worn on the surface of the eye in children who have myopia to:  •\tReduce the rate of progression of myopia, and  •\tOptically correct myopic refractive error.",
      "regulation_number": "",
      "implant_flag": "N",
      "submission_type_id": "2"
    }
  ]
}