FDA 510(k)

費林-針刺器

K 號：K153243 · 2016-08-04

決定日期2016-08-04

產品代碼HAE

諮詢委員會NE (請提供完整的英文描述，以便進行翻譯。)

決定相當於

器材摘要

Fehling-Punches is the device name listed in this FDA 510(k) record. The listed applicant is Fehling Instruments GmbH & Co. KG. It received FDA 510(k) clearance on 2016-08-04 under 510(k) number K153243. The device is classified under product code HAE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Fehling-Punches?

Fehling-Punches is a medical device that received FDA 510(k) clearance on 2016-08-04. The listed applicant is Fehling Instruments GmbH & Co. KG. The 510(k) number is K153243.

When did Fehling-Punches receive FDA 510(k) clearance?

Fehling-Punches received FDA 510(k) clearance on 2016-08-04, under 510(k) number K153243.

Who is the listed applicant for Fehling-Punches?

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

What is the FDA product code for Fehling-Punches?

The FDA product code for Fehling-Punches is HAE.

其他以 Fehling Instruments GmbH & Co. KG 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。

K170726組織切片镊子

相關器械（代碼：HAE）

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。

K260446Tontarra 打擊器與磨削器Tontarra Medizintechnik GmbH K242759Geister K-Rex 適應性咬合器Geister Medizin Technik GmbH K223596SQ.line 賽里遜Aesculap, Inc.K230256叛亂，幻影多咬合凱遜鋸齒刀Morpheus AG K221818叛亂；幻影多咬式凱遜咬骨器Morpheus AG K210741KLS Martin 神經鍵盤KLS-Martin L.P.

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。