{
  "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": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "QFT",
      "openfda": {
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      "device_name": "Digital Therapeutic Software For Attention Deficit Hyperactivity Disorder",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Obstetrics/Gynecology",
      "device_class": "2",
      "definition": "A digital therapy device for Attention Deficit Hyperactivity Disorder (ADHD) is a software intended to provide therapy for ADHD or any of its individual symptoms as an adjunct to clinician supervised treatment.",
      "regulation_number": "882.5803",
      "implant_flag": "N",
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}