FDA 510(k)

mollosil 超級

K 號：K162654 · 2017-03-13

決定日期2017-03-13

產品代碼EBI

諮詢委員會DE

決定相當於

器材摘要

mollosil plus is the device name listed in this FDA 510(k) record. The listed applicant is Detax GmbH & Co. KG. It received FDA 510(k) clearance on 2017-03-13 under 510(k) number K162654. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the mollosil plus?

mollosil plus is a medical device that received FDA 510(k) clearance on 2017-03-13. The listed applicant is Detax GmbH & Co. KG. The 510(k) number is K162654.

When did mollosil plus receive FDA 510(k) clearance?

mollosil plus received FDA 510(k) clearance on 2017-03-13, under 510(k) number K162654.

Who is the listed applicant for mollosil plus?

The FDA 510(k) record lists Detax GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for mollosil plus?

The FDA product code for mollosil plus is EBI.

其他以 Detax GmbH & Co. KG 為申請人之記錄

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相關器械（代碼：EBI）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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