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FDA 510(k)

PowerPICC Provena Catheters

K号: K162443 · 2016-10-25

决定日期2016-10-25
产品代码LJS
咨询委员会HO
决定Substantially Equivalent

器械摘要

PowerPICC Provena Catheters is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2016-10-25 under 510(k) number K162443. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the PowerPICC Provena Catheters?

PowerPICC Provena Catheters is a medical device that received FDA 510(k) clearance on 2016-10-25. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K162443.

When did PowerPICC Provena Catheters receive FDA 510(k) clearance?

PowerPICC Provena Catheters received FDA 510(k) clearance on 2016-10-25, under 510(k) number K162443.

Who is the listed applicant for PowerPICC Provena Catheters?

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

What is the FDA product code for PowerPICC Provena Catheters?

The FDA product code for PowerPICC Provena Catheters is LJS.

相关临床试验

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列明C.R. Bard, Inc.为申报人的其他记录

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相关器械(代码:LJS)

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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