3合1经皮神经电刺激仪(TC1241,TC2241,TS1241)
K号: K251187 · 2025-07-28
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器械摘要
常见问题
What is the 3 in 1 TENS UNIT (TC1241, TC2241, TS1241)?
3 in 1 TENS UNIT (TC1241, TC2241, TS1241) is a medical device that received FDA 510(k) clearance on 2025-07-28. The listed applicant is Changsha Anxiang Medical Technology Co., Ltd.. The 510(k) number is K251187.
When did 3 in 1 TENS UNIT (TC1241, TC2241, TS1241) receive FDA 510(k) clearance?
3 in 1 TENS UNIT (TC1241, TC2241, TS1241) received FDA 510(k) clearance on 2025-07-28, under 510(k) number K251187.
Who is the listed applicant for 3 in 1 TENS UNIT (TC1241, TC2241, TS1241)?
The FDA 510(k) record lists Changsha Anxiang Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 3 in 1 TENS UNIT (TC1241, TC2241, TS1241)?
The FDA product code for 3 in 1 TENS UNIT (TC1241, TC2241, TS1241) is NUH.
列明Changsha Anxiang Medical Technology Co., Ltd.为申报人的其他记录
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
相关器械(代码:NUH)
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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