{
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    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-10-12",
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      "applicant": "Boston Scientific Corporation",
      "street_1": "4100 Hamline Ave. N",
      "street_2": "",
      "city": "St Paul",
      "state": "MN",
      "zip": "55112",
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      "generic_name": "Implantable cardioverter defibrillator (non-CRT)",
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      "supplement_type": "30-Day Notice",
      "supplement_reason": "Process Change - Manufacturer/Sterilizer/Packager/Supplier",
      "expedited_review_flag": "N",
      "date_received": "2026-09-10",
      "decision_date": "2026-10-02",
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      "decision_code": "OK30",
      "ao_statement": "to adjust the manufacturing steps and modify the laser equipment software for the HV capacitors in EMBLEM SICD devices",
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