FDA 510(k)

eego放大器

K号: K172312 · 2018-03-30

申请人Eemagine Medical Imaging Solutions GmbH

决定日期2018-03-30

产品代码GWL

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决定实质等同

器械摘要

eego amplifiers is the device name listed in this FDA 510(k) record. The listed applicant is Eemagine Medical Imaging Solutions GmbH. It received FDA 510(k) clearance on 2018-03-30 under 510(k) number K172312. The device is classified under product code GWL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the eego amplifiers?

eego amplifiers is a medical device that received FDA 510(k) clearance on 2018-03-30. The listed applicant is Eemagine Medical Imaging Solutions GmbH. The 510(k) number is K172312.

When did eego amplifiers receive FDA 510(k) clearance?

eego amplifiers received FDA 510(k) clearance on 2018-03-30, under 510(k) number K172312.

Who is the listed applicant for eego amplifiers?

The FDA 510(k) record lists Eemagine Medical Imaging Solutions GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for eego amplifiers?

The FDA product code for eego amplifiers is GWL.

列明Eemagine Medical Imaging Solutions GmbH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。

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