K241156
- 510(k) 号
- K241156
- 器械名称
- Medline ReNewal Reprocessed St. Jude Medical Response Electrophysiology Catheter, Supreme Electrophysiology Catheter (401150, 401206, 401207, 401210, 401211, 401212, 401222, 401223, 401226, 401227, 401228, 401260, 401261, 401271, 401305, 401306, 401309, 401310, 401311, 401312, 401317, 401353, 401357, 401381, 401392, 401399, 401400, 401425, 401430, 401433, 401434, 401435, 401436, 401438, 401441, 401442, 401443, 401444, 401445, 401448, 401449, 401450, 401451, 401453, 401466, 401468, 401
- 申请人
- Surgical Instrument Service and Savings, Inc. OR · US
- 产品代码
- NLH — Catheter, Recording, Electrode, Reprocessed
- 批准日期
- 2024-09-14
- 受理日期
- 2024-04-26
- 决定
- Substantially Equivalent
- 审查途径
- Traditional
- 咨询委员会
- Cardiovascular
FDA 官方记录: K241156
数据来自 openFDA 510(k) 数据集(CC0 公有领域),以 FDA 现行记录为准。510(k) 许可不等于 FDA 认证或批准。