{
  "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",
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      "applicant": "Guidant Corp.",
      "street_1": "4100 Hamline Ave. N",
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      "city": "St Paul",
      "state": "MN",
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      "advisory_committee_description": "Cardiovascular",
      "supplement_type": "30-Day Notice",
      "supplement_reason": "Process Change - Manufacturer/Sterilizer/Packager/Supplier",
      "expedited_review_flag": "N",
      "date_received": "2026-06-26",
      "decision_date": "2026-07-23",
      "docket_number": "",
      "decision_code": "OK30",
      "ao_statement": "to add a functionally equivalent alternate vapor degreasing solvent used to remove contaminants from pulse generator components",
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