K254200
- 510(k) 号
- K254200
- 器械名称
- Air Compression Leg Massager (LF-FT001, LF-FT002-1, LF-FT003, LF-FT003-1, LF-FT004-1, LF-FT005-1, LF-FT006-1, LF-FT007, LF-FT008, LF-FT009, LF-FT010, LF-FT011, LF-FT012, LF-FT013, LF-FT014, LF-FT015, LF-FT016, UM-01, UM-02, UM-03, UM-03-1, UM-04-1, UM-05-1, UM-06-1, UM-07, UM-08, UM-09, UM-10, UM-11, UM-12, UM-13, UM-14, UM-15, UM-16, AI-01, AI-02, AI-03, AI-04, AI-05, AI-06, AI01, AI02, AI03, AI-07, AI-08, AI-09, AI-10, AI-11, AI-12, AI-13, AI-14)
- 申请人
- Wenzhou Lingfeng Electronic Technology Co., Ltd. CN
- 产品代码
- IRP — Massager, Powered Inflatable Tube
- 批准日期
- 2026-05-05
- 受理日期
- 2025-12-29
- 决定
- Substantially Equivalent
- 审查途径
- Traditional
- 咨询委员会
- Physical Medicine
FDA 官方记录: K254200
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。