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FDA 510(k)

人機工程學把手

K 號:K173272 · 2018-02-09

決定日期2018-02-09
產品代碼GCJ
諮詢委員會GU
決定相當於

器材摘要

Ergonomic Handle is the device name listed in this FDA 510(k) record. The listed applicant is Symmetry Surgical, Inc.. It received FDA 510(k) clearance on 2018-02-09 under 510(k) number K173272. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Ergonomic Handle?

Ergonomic Handle is a medical device that received FDA 510(k) clearance on 2018-02-09. The listed applicant is Symmetry Surgical, Inc.. The 510(k) number is K173272.

When did Ergonomic Handle receive FDA 510(k) clearance?

Ergonomic Handle received FDA 510(k) clearance on 2018-02-09, under 510(k) number K173272.

Who is the listed applicant for Ergonomic Handle?

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

What is the FDA product code for Ergonomic Handle?

The FDA product code for Ergonomic Handle is GCJ.

相關臨床試驗

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其他以 Symmetry Surgical, 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。

相關器械(代碼:GCJ)

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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