FDA 510(k)

和諧鉤

K 號：K151136 · 2016-03-04

決定日期2016-03-04

產品代碼LFL

決定相當於

器材摘要

HARMONIC HOOK is the device name listed in this FDA 510(k) record. The listed applicant is Ethicon Endo-Surgery, LLC. It received FDA 510(k) clearance on 2016-03-04 under 510(k) number K151136. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

常見問題

What is the HARMONIC HOOK?

HARMONIC HOOK is a medical device that received FDA 510(k) clearance on 2016-03-04. The listed applicant is Ethicon Endo-Surgery, LLC. The 510(k) number is K151136.

When did HARMONIC HOOK receive FDA 510(k) clearance?

HARMONIC HOOK received FDA 510(k) clearance on 2016-03-04, under 510(k) number K151136.

Who is the listed applicant for HARMONIC HOOK?

FDA 510(k) 記錄中將 Ethicon Endo-Surgery, LLC 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for HARMONIC HOOK?

The FDA product code for HARMONIC HOOK is LFL.

其他以 Ethicon Endo-Surgery, LLC 為申請人之記錄

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相關器械（代碼：LFL）

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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