{
  "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": "2026-10-05",
    "results": {
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      "pma_number": "P010030",
      "supplement_number": "",
      "applicant": "Zoll Manufacturing Corporation",
      "street_1": "121 Gamma Dr.",
      "street_2": "",
      "city": "Pittsburgh",
      "state": "PA",
      "zip": "15238",
      "zip_ext": "",
      "generic_name": "Wearable automated external defibrillator",
      "trade_name": "WEARABLE CARDIOVERTER DEFIBRILLATOR (WCD) 2000 LIFEVEST",
      "product_code": "MVK",
      "advisory_committee": "CV",
      "advisory_committee_description": "Cardiovascular",
      "supplement_type": "",
      "supplement_reason": "",
      "expedited_review_flag": "N",
      "date_received": "2001-05-04",
      "decision_date": "2001-12-18",
      "docket_number": "02M-0145",
      "fed_reg_notice_date": "2002-04-12",
      "decision_code": "APPR",
      "ao_statement": "APPROVAL FOR THE WCD 2000 SYSTEM.  THIS DEVICE IS INDICATED FOR ADULT PATIENTS WHO ARE AT RISK FOR SUDDEN CARDIAC ARREST AND EITHER ARE NOT CANDIDATES FOR OR REFUSE AN IMPLANTABLE DEFIBRILLATOR.",
      "openfda": {
        "device_name": "Wearable Automated External Defibrillator",
        "medical_specialty_description": "Unknown",
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        "device_class": "3",
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