FDA 510(k)

ERBE ESU Model VIO dV 及附件

K号: K150364 · 2016-05-05

决定日期2016-05-05

产品代码GEI

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决定实质等同

器械摘要

ERBE ESU Model VIO dV with Accessories is the device name listed in this FDA 510(k) record. The listed applicant is Erbe Elektromedizin GmbH. It received FDA 510(k) clearance on 2016-05-05 under 510(k) number K150364. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ERBE ESU Model VIO dV with Accessories?

ERBE ESU Model VIO dV with Accessories is a medical device that received FDA 510(k) clearance on 2016-05-05. The listed applicant is Erbe Elektromedizin GmbH. The 510(k) number is K150364.

When did ERBE ESU Model VIO dV with Accessories receive FDA 510(k) clearance?

ERBE ESU Model VIO dV with Accessories received FDA 510(k) clearance on 2016-05-05, under 510(k) number K150364.

Who is the listed applicant for ERBE ESU Model VIO dV with Accessories?

The FDA 510(k) record lists Erbe Elektromedizin GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ERBE ESU Model VIO dV with Accessories?

The FDA product code for ERBE ESU Model VIO dV with Accessories is GEI.

列明Erbe Elektromedizin 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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相关器械（代码：GEI）

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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