{
  "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": "San Francisco",
      "advisory_committee_description": "Neurology",
      "address_1": "201 Mission St. #1450",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "QVO",
      "openfda": {
        "device_name": "Computerized Behavioral Therapy Device For Insomnia",
        "medical_specialty_description": "Neurology",
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      "applicant": "Pear Therapeutics, Inc.",
      "decision_date": "2020-03-23",
      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "Somryst",
      "advisory_committee": "NE",
      "contact": "David  Amor",
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      "k_number": "K191716",
      "state": "CA",
      "date_received": "2019-06-26",
      "review_advisory_committee": "NE",
      "postal_code": "94105",
      "decision_description": "Substantially Equivalent",
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  ]
}