FDA 510(k)

凈膠通用應用膠

K 號：K153174 · 2016-04-13

決定日期2016-04-13

產品代碼EMA

諮詢委員會DE

決定相當於

器材摘要

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.

常見問題

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.

其他以 3M Deutschland GmbH 為申請人之記錄

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相關器械（代碼：EMA）

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