FDA 510(k)

SpyGlass Discover 激光擴張導管

K 號：K212582 · 2022-05-06

決定日期2022-05-06

產品代碼GCA

諮詢委員會GU

決定相當於

器材摘要

SpyGlass Discover Balloon Dilation Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corporation. It received FDA 510(k) clearance on 2022-05-06 under 510(k) number K212582. The device is classified under product code GCA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the SpyGlass Discover Balloon Dilation Catheter?

SpyGlass Discover Balloon Dilation Catheter is a medical device that received FDA 510(k) clearance on 2022-05-06. The listed applicant is Boston Scientific Corporation. The 510(k) number is K212582.

When did SpyGlass Discover Balloon Dilation Catheter receive FDA 510(k) clearance?

SpyGlass Discover Balloon Dilation Catheter received FDA 510(k) clearance on 2022-05-06, under 510(k) number K212582.

Who is the listed applicant for SpyGlass Discover Balloon Dilation Catheter?

FDA 510(k) 記錄中將波士頓科學公司列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for SpyGlass Discover Balloon Dilation Catheter?

The FDA product code for SpyGlass Discover Balloon Dilation Catheter is GCA.

其他以 Boston Scientific Corporation 為申請人之記錄

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相關器械（代碼：GCA）

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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官方來源

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