{
  "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": "2026-08-17",
    "results": {
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      "supplement_number": "S001",
      "applicant": "Kardium, Inc.",
      "street_1": "8518 Glenlyon Pkwy.",
      "street_2": "Unit 155",
      "city": "Burnaby",
      "state": "",
      "zip": "V5J OB6",
      "zip_ext": "",
      "generic_name": "Percutaneous Cardiac Ablation Catheter for Treatment of Atrial Fibrillation with Irreversible Electroporation",
      "trade_name": "Globe® Catheter and Globe® Pulsed Field System",
      "product_code": "QZI",
      "advisory_committee": "CV",
      "advisory_committee_description": "Cardiovascular",
      "supplement_type": "Normal 180 Day Track No User Fee",
      "supplement_reason": "Postapproval Study Protocol",
      "expedited_review_flag": "N",
      "date_received": "2025-09-29",
      "decision_date": "2026-06-23",
      "docket_number": "",
      "decision_code": "APPR",
      "ao_statement": "approval of the protocol for the post-approval study (PAS) referenced above. The PAS protocol has been submitted to comply with the conditions of approval outlined in our approval order for P240044",
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        "medical_specialty_description": "Unknown",
        "regulation_number": "",
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