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FDA 510(k)

SwiftNINJA Microcatheter

K号: K161921 · 2016-11-04

决定日期2016-11-04
产品代码KRA
咨询委员会CV
决定Substantially Equivalent

器械摘要

SwiftNINJA Microcatheter is the device name listed in this FDA 510(k) record. The listed applicant is Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 2016-11-04 under 510(k) number K161921. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the SwiftNINJA Microcatheter?

SwiftNINJA Microcatheter is a medical device that received FDA 510(k) clearance on 2016-11-04. The listed applicant is Merit Medical Systems, Inc.. The 510(k) number is K161921.

When did SwiftNINJA Microcatheter receive FDA 510(k) clearance?

SwiftNINJA Microcatheter received FDA 510(k) clearance on 2016-11-04, under 510(k) number K161921.

Who is the listed applicant for SwiftNINJA Microcatheter?

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

What is the FDA product code for SwiftNINJA Microcatheter?

The FDA product code for SwiftNINJA Microcatheter is KRA.

相关临床试验

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列明Merit Medical Systems, Inc.为申报人的其他记录

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相关器械(代码:KRA)

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

官方来源

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