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FDA 510(k)

POWERSEAL 封口器和分隔器

K号: K231327 · 2023-10-25

决定日期2023-10-25
产品代码GEI
咨询委员会SU 请注意,您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同

器械摘要

POWERSEAL Sealer and Divider is the device name listed in this FDA 510(k) record. The listed applicant is Gyrus Acmi, Inc.. It received FDA 510(k) clearance on 2023-10-25 under 510(k) number K231327. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the POWERSEAL Sealer and Divider?

POWERSEAL Sealer and Divider is a medical device that received FDA 510(k) clearance on 2023-10-25. The listed applicant is Gyrus Acmi, Inc.. The 510(k) number is K231327.

When did POWERSEAL Sealer and Divider receive FDA 510(k) clearance?

POWERSEAL Sealer and Divider received FDA 510(k) clearance on 2023-10-25, under 510(k) number K231327.

Who is the listed applicant for POWERSEAL Sealer and Divider?

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

What is the FDA product code for POWERSEAL Sealer and Divider?

The FDA product code for POWERSEAL Sealer and Divider is GEI.

相关临床试验

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列明Gyrus Acmi, Inc.为申报人的其他记录

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相关器械(代码:GEI)

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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