FDA 510(k)

EasyClip® 及 EasyClip® Xpress

K 號：K210582 · 2022-06-10

決定日期2022-06-10

產品代碼JDR

諮詢委員會或

決定相當於

器材摘要

EasyClip® and EasyClip® Xpress is the device name listed in this FDA 510(k) record. The listed applicant is Stryker GmbH. It received FDA 510(k) clearance on 2022-06-10 under 510(k) number K210582. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the EasyClip® and EasyClip® Xpress?

EasyClip® and EasyClip® Xpress is a medical device that received FDA 510(k) clearance on 2022-06-10. The listed applicant is Stryker GmbH. The 510(k) number is K210582.

When did EasyClip® and EasyClip® Xpress receive FDA 510(k) clearance?

EasyClip® and EasyClip® Xpress received FDA 510(k) clearance on 2022-06-10, under 510(k) number K210582.

Who is the listed applicant for EasyClip® and EasyClip® Xpress?

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

What is the FDA product code for EasyClip® and EasyClip® Xpress?

The FDA product code for EasyClip® and EasyClip® Xpress is JDR.

其他以 Stryker GmbH 為申請人之記錄

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相關器械（代碼：JDR）

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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