FDA 510(k)

單次使用線性切釘器及裝填單位，單次使用圓形釘釘器

K 號：K182217 · 2019-04-16

決定日期2019-04-16

產品代碼GDW

諮詢委員會SU 請提供完整的描述文本，以便我進行翻譯。

決定相當於

器材摘要

Linear Cutter Staplers and Loading Units for Single Use, Circular Staplers for Single Use is the device name listed in this FDA 510(k) record. The listed applicant is Ezisurg (Suzhou) Medical Co., Ltd.. It received FDA 510(k) clearance on 2019-04-16 under 510(k) number K182217. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Linear Cutter Staplers and Loading Units for Single Use, Circular Staplers for Single Use?

Linear Cutter Staplers and Loading Units for Single Use, Circular Staplers for Single Use is a medical device that received FDA 510(k) clearance on 2019-04-16. The listed applicant is Ezisurg (Suzhou) Medical Co., Ltd.. The 510(k) number is K182217.

When did Linear Cutter Staplers and Loading Units for Single Use, Circular Staplers for Single Use receive FDA 510(k) clearance?

Linear Cutter Staplers and Loading Units for Single Use, Circular Staplers for Single Use received FDA 510(k) clearance on 2019-04-16, under 510(k) number K182217.

Who is the listed applicant for Linear Cutter Staplers and Loading Units for Single Use, Circular Staplers for Single Use?

The FDA 510(k) record lists Ezisurg (Suzhou) Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Linear Cutter Staplers and Loading Units for Single Use, Circular Staplers for Single Use?

The FDA product code for Linear Cutter Staplers and Loading Units for Single Use, Circular Staplers for Single Use is GDW.

其他以 Ezisurg (Suzhou) Medical Co., Ltd. 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。

K181620內視鏡線性切釘器及單次使用裝填單位

相關器械（代碼：GDW）

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。

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。