经皮神经电刺激(TENS)和电肌肉刺激器(型号:KRES100D, KRES1010, KRES1020, KRES1080)
K号: K213788 · 2022-05-06
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器械摘要
常见问题
What is the TENS&EMS STIMULATOR (Model: KRES100D, KRES1010, KRES1020, KRES1080)?
TENS&EMS STIMULATOR (Model: KRES100D, KRES1010, KRES1020, KRES1080) is a medical device that received FDA 510(k) clearance on 2022-05-06. The listed applicant is Dongguan Bohuikang Technology Co.,Ltd. The 510(k) number is K213788.
When did TENS&EMS STIMULATOR (Model: KRES100D, KRES1010, KRES1020, KRES1080) receive FDA 510(k) clearance?
TENS&EMS STIMULATOR (Model: KRES100D, KRES1010, KRES1020, KRES1080) received FDA 510(k) clearance on 2022-05-06, under 510(k) number K213788.
Who is the listed applicant for TENS&EMS STIMULATOR (Model: KRES100D, KRES1010, KRES1020, KRES1080)?
The FDA 510(k) record lists Dongguan Bohuikang Technology Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TENS&EMS STIMULATOR (Model: KRES100D, KRES1010, KRES1020, KRES1080)?
The FDA product code for TENS&EMS STIMULATOR (Model: KRES100D, KRES1010, KRES1020, KRES1080) is NUH.
相关临床试验
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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