FDA 510(k)

瓷美儂 A-Temp

K 號：K191843 · 2019-10-04

決定日期2019-10-04

產品代碼EBG

諮詢委員會DE

決定相當於

器材摘要

Ceramill A-Temp is the device name listed in this FDA 510(k) record. The listed applicant is Amann Girrbach AG. It received FDA 510(k) clearance on 2019-10-04 under 510(k) number K191843. 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 Ceramill A-Temp?

Ceramill A-Temp is a medical device that received FDA 510(k) clearance on 2019-10-04. The listed applicant is Amann Girrbach AG. The 510(k) number is K191843.

When did Ceramill A-Temp receive FDA 510(k) clearance?

Ceramill A-Temp received FDA 510(k) clearance on 2019-10-04, under 510(k) number K191843.

Who is the listed applicant for Ceramill A-Temp?

The FDA 510(k) record lists Amann Girrbach AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ceramill A-Temp?

The FDA product code for Ceramill A-Temp is EBG.

其他以 Amann Girrbach AG 為申請人之記錄

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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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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