FDA 510(k)

Ketac Universal Aplicap

K号: K153174 · 2016-04-13

决定日期2016-04-13

产品代码EMA

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决定实质等同

器械摘要

Ketac Universal Aplicap 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 2016-04-13 under 510(k) number K153174. 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 Ketac Universal Aplicap?

Ketac Universal Aplicap is a medical device that received FDA 510(k) clearance on 2016-04-13. The listed applicant is 3M Deutschland GmbH. The 510(k) number is K153174.

When did Ketac Universal Aplicap receive FDA 510(k) clearance?

Ketac Universal Aplicap received FDA 510(k) clearance on 2016-04-13, under 510(k) number K153174.

Who is the listed applicant for Ketac Universal Aplicap?

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 Ketac Universal Aplicap?

The FDA product code for Ketac Universal Aplicap is EMA.

列明3M Deutschland GmbH为申报人的其他记录

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