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FDA 510(k)

BRH-A2 联合超声和电场刺激(CUSEFS)

K号: K160378 · 2017-08-25

决定日期2017-08-25
产品代码IMI
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决定实质等同

器械摘要

BRH-A2 Combined Ultrasound and Electric Field Stimulation (CUSEFS) is the device name listed in this FDA 510(k) record. The listed applicant is Brh Medical , Ltd.. It received FDA 510(k) clearance on 2017-08-25 under 510(k) number K160378. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BRH-A2 Combined Ultrasound and Electric Field Stimulation (CUSEFS)?

BRH-A2 Combined Ultrasound and Electric Field Stimulation (CUSEFS) is a medical device that received FDA 510(k) clearance on 2017-08-25. The listed applicant is Brh Medical , Ltd.. The 510(k) number is K160378.

When did BRH-A2 Combined Ultrasound and Electric Field Stimulation (CUSEFS) receive FDA 510(k) clearance?

BRH-A2 Combined Ultrasound and Electric Field Stimulation (CUSEFS) received FDA 510(k) clearance on 2017-08-25, under 510(k) number K160378.

Who is the listed applicant for BRH-A2 Combined Ultrasound and Electric Field Stimulation (CUSEFS)?

The FDA 510(k) record lists Brh Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BRH-A2 Combined Ultrasound and Electric Field Stimulation (CUSEFS)?

The FDA product code for BRH-A2 Combined Ultrasound and Electric Field Stimulation (CUSEFS) is IMI.

相关临床试验

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相关器械(代码:IMI)

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。

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