FDA 510(k)

Expro Elite 銳圈，Sympro Elite 銳圈

K 號：K163307 · 2017-03-08

決定日期2017-03-08

產品代碼MMX

諮詢委員會履歷

決定相當於

器材摘要

Expro Elite Snare, Sympro Elite Snare is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Solutions, Inc.. It received FDA 510(k) clearance on 2017-03-08 under 510(k) number K163307. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Expro Elite Snare, Sympro Elite Snare?

Expro Elite Snare, Sympro Elite Snare is a medical device that received FDA 510(k) clearance on 2017-03-08. The listed applicant is Vascular Solutions, Inc.. The 510(k) number is K163307.

When did Expro Elite Snare, Sympro Elite Snare receive FDA 510(k) clearance?

Expro Elite Snare, Sympro Elite Snare received FDA 510(k) clearance on 2017-03-08, under 510(k) number K163307.

Who is the listed applicant for Expro Elite Snare, Sympro Elite Snare?

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

What is the FDA product code for Expro Elite Snare, Sympro Elite Snare?

The FDA product code for Expro Elite Snare, Sympro Elite Snare is MMX.

其他以 Vascular Solutions, Inc. 為申請人之記錄

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相關器械（代碼：MMX）

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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