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FDA 510(k)

Oscar 外周多功能导管系统

K号: K214038 · 2022-07-06

决定日期2022-07-06
产品代码LIT
咨询委员会CV
决定Substantially Equivalent

器械摘要

Oscar Peripheral Multifunctional Catheter system is the device name listed in this FDA 510(k) record. The listed applicant is Biotronik, Inc.. It received FDA 510(k) clearance on 2022-07-06 under 510(k) number K214038. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Oscar Peripheral Multifunctional Catheter system?

Oscar Peripheral Multifunctional Catheter system is a medical device that received FDA 510(k) clearance on 2022-07-06. The listed applicant is Biotronik, Inc.. The 510(k) number is K214038.

When did Oscar Peripheral Multifunctional Catheter system receive FDA 510(k) clearance?

Oscar Peripheral Multifunctional Catheter system received FDA 510(k) clearance on 2022-07-06, under 510(k) number K214038.

Who is the listed applicant for Oscar Peripheral Multifunctional Catheter system?

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

What is the FDA product code for Oscar Peripheral Multifunctional Catheter system?

The FDA product code for Oscar Peripheral Multifunctional Catheter system is LIT.

相关临床试验

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列明Biotronik, Inc.为申报人的其他记录

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相关器械(代码:LIT)

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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