{
  "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": "2026-04-13",
    "results": {
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      "third_party_flag": "N",
      "city": "Minneapolis",
      "advisory_committee_description": "Cardiovascular",
      "address_1": "7000 Central Ave., NE",
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      "statement_or_summary": "Summary",
      "product_code": "MXC",
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      "device_name": "REVEAL PLUS INSERTABLE LOOP RECORDER SYSTEM MODEL 9526 IMPLANTABLE RECORDER AND MODEL 6191 PATIENT ACTIVATOR",
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}