FDA 510(k)

明顯臨時C&B

K 號：K192830 · 2020-09-02

決定日期2020-09-02

產品代碼EBG

諮詢委員會DE

決定相當於

器材摘要

Bright Temporary C&B is the device name listed in this FDA 510(k) record. The listed applicant is Dmp Dental Industry S.A.. It received FDA 510(k) clearance on 2020-09-02 under 510(k) number K192830. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Bright Temporary C&B?

Bright Temporary C&B is a medical device that received FDA 510(k) clearance on 2020-09-02. The listed applicant is Dmp Dental Industry S.A.. The 510(k) number is K192830.

When did Bright Temporary C&B receive FDA 510(k) clearance?

Bright Temporary C&B received FDA 510(k) clearance on 2020-09-02, under 510(k) number K192830.

Who is the listed applicant for Bright Temporary C&B?

The FDA 510(k) record lists Dmp Dental Industry S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bright Temporary C&B?

The FDA product code for Bright Temporary C&B is EBG.

其他以 Dmp Dental Industry S.A. 為申請人之記錄

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相關器械（代碼：EBG）

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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