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FDA 510(k)

Entuit PEG,Entuit PEGJ

K号: K213356 · 2022-01-20

决定日期2022-01-20
产品代码PIF
咨询委员会GU 请注意,由于您只提供了“GU”这个词,我无法提供完整的翻译。如果您能提供完整的句子或段落,我将能够为您提供准确的翻译。
决定Unknown

器械摘要

Entuit PEG, Entuit PEGJ is the device name listed in this FDA 510(k) record. The listed applicant is Wilson-Cook Medical, Inc.. It received FDA 510(k) clearance on 2022-01-20 under 510(k) number K213356. The device is classified under product code PIF. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

常见问题

What is the Entuit PEG, Entuit PEGJ?

Entuit PEG, Entuit PEGJ is a medical device that received FDA 510(k) clearance on 2022-01-20. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K213356.

When did Entuit PEG, Entuit PEGJ receive FDA 510(k) clearance?

Entuit PEG, Entuit PEGJ received FDA 510(k) clearance on 2022-01-20, under 510(k) number K213356.

Who is the listed applicant for Entuit PEG, Entuit PEGJ?

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

What is the FDA product code for Entuit PEG, Entuit PEGJ?

The FDA product code for Entuit PEG, Entuit PEGJ is PIF.

相关临床试验

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列明Wilson-Cook Medical, Inc.为申报人的其他记录

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查看所有 32 个设备 →

相关器械(代码:PIF)

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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