{
  "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": "2026-10-19",
    "results": {
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Toronto",
      "advisory_committee_description": "Cardiovascular",
      "address_1": "160 Bloor St. E.",
      "address_2": "Suite 910",
      "statement_or_summary": "Summary",
      "product_code": "SAT",
      "openfda": {
        "device_name": "Pulmonary Hypertension Machine Learning-Based Notification Software",
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        "regulation_number": "870.2380",
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      "country_code": "CA",
      "device_name": "CorVista System with PH Add-On",
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      "contact": "Gabrielle  Zaeska",
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      "k_number": "K233666",
      "state": "",
      "date_received": "2023-11-15",
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      "decision_description": "Substantially Equivalent",
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}