K250517
- 510(k) 号
- K250517
- 器械名称
- Navigator HD Ureteral Access Sheath Set 11/13 F x 28cm (M0062502210); Navigator HD Ureteral Access Sheath Set 11/13 F x 36cm (M0062502220); Navigator HD Ureteral Access Sheath Set 11/13 F x 46cm (M0062502230); Navigator HD Ureteral Access Sheath Set 12/14 F x 28cm (M0062502240); Navigator HD Ureteral Access Sheath Set 12/14 F x 36cm (M0062502250); Navigator HD Ureteral Access Sheath Set 12/14 F x 46cm (M0062502260); Navigator HD Ureteral Access Sheath Set 13/15 F x 28cm (M006
- 申请人
- Boston Scientific Corporation MA · US
- 产品代码
- FED — Endoscopic Access Overtube, Gastroenterology-Urology
- 批准日期
- 2025-03-21
- 受理日期
- 2025-02-21
- 决定
- Substantially Equivalent
- 审查途径
- Special
- 咨询委员会
- Gastroenterology, Urology
FDA 官方记录: K250517
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。