FDA 510(k)

ELAN 4 工具

K 號：K182527 · 2019-01-19

決定日期2019-01-19

產品代碼HBE

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

ELAN 4 Tools is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2019-01-19 under 510(k) number K182527. The device is classified under product code HBE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ELAN 4 Tools?

ELAN 4 Tools is a medical device that received FDA 510(k) clearance on 2019-01-19. The listed applicant is Aesculap, Inc.. The 510(k) number is K182527.

When did ELAN 4 Tools receive FDA 510(k) clearance?

ELAN 4 Tools received FDA 510(k) clearance on 2019-01-19, under 510(k) number K182527.

Who is the listed applicant for ELAN 4 Tools?

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

What is the FDA product code for ELAN 4 Tools?

The FDA product code for ELAN 4 Tools is HBE.

其他以 Aesculap, Inc. 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。

K242762Aesculap Aicon® 系列容器系統 K242003XABO 心室針，XABO 腹膜針，XABO 針套組 K223596SQ.line 賽里遜 K214041Aesculap AICON 容器 K211572Aesculap Slim Clip Applier K203739ELAN 4 電機系統

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相關器械（代碼：HBE）

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

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