FDA 510(k)

Suglue 3

K号: K192992 · 2019-11-05

决定日期2019-11-05

产品代码EMA

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决定实质等同

器械摘要

Suglue 3 is the device name listed in this FDA 510(k) record. The listed applicant is 3M Deutschland GmbH. It received FDA 510(k) clearance on 2019-11-05 under 510(k) number K192992. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Suglue 3?

Suglue 3 is a medical device that received FDA 510(k) clearance on 2019-11-05. The listed applicant is 3M Deutschland GmbH. The 510(k) number is K192992.

When did Suglue 3 receive FDA 510(k) clearance?

Suglue 3 received FDA 510(k) clearance on 2019-11-05, under 510(k) number K192992.

Who is the listed applicant for Suglue 3?

The FDA 510(k) record lists 3M Deutschland GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Suglue 3?

The FDA product code for Suglue 3 is EMA.

列明3M Deutschland 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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