FDA 510(k)

RIST 心臟內科用長型放射學桡骨進入鞘

K 號：K191551 · 2019-12-23

決定日期2019-12-23

產品代碼DQY

諮詢委員會履歷

決定相當於

器材摘要

RIST Cath Radial Access Long Sheath is the device name listed in this FDA 510(k) record. The listed applicant is Rist Neurovascular, Inc.. It received FDA 510(k) clearance on 2019-12-23 under 510(k) number K191551. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the RIST Cath Radial Access Long Sheath?

RIST Cath Radial Access Long Sheath is a medical device that received FDA 510(k) clearance on 2019-12-23. The listed applicant is Rist Neurovascular, Inc.. The 510(k) number is K191551.

When did RIST Cath Radial Access Long Sheath receive FDA 510(k) clearance?

RIST Cath Radial Access Long Sheath received FDA 510(k) clearance on 2019-12-23, under 510(k) number K191551.

Who is the listed applicant for RIST Cath Radial Access Long Sheath?

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

What is the FDA product code for RIST Cath Radial Access Long Sheath?

The FDA product code for RIST Cath Radial Access Long Sheath is DQY.

其他以 Rist Neurovascular, 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。

K201682RIST 體外循環導管 K200417RIST 體外循環導管

相關器械（代碼：DQY）

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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