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FDA 510(k)

Signia™ 小直径重装包括常规（圆形）尖端版本

K号: K222641 · 2022-11-29

申请人Covidien
决定日期2022-11-29
产品代码GDW
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

Signia™ Small Diameter Reloads Including Regular (Round) Tip Version is the device name listed in this FDA 510(k) record. The listed applicant is Covidien. It received FDA 510(k) clearance on 2022-11-29 under 510(k) number K222641. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Signia™ Small Diameter Reloads Including Regular (Round) Tip Version?

Signia™ Small Diameter Reloads Including Regular (Round) Tip Version is a medical device that received FDA 510(k) clearance on 2022-11-29. The listed applicant is Covidien. The 510(k) number is K222641.

When did Signia™ Small Diameter Reloads Including Regular (Round) Tip Version receive FDA 510(k) clearance?

Signia™ Small Diameter Reloads Including Regular (Round) Tip Version received FDA 510(k) clearance on 2022-11-29, under 510(k) number K222641.

Who is the listed applicant for Signia™ Small Diameter Reloads Including Regular (Round) Tip Version?

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

What is the FDA product code for Signia™ Small Diameter Reloads Including Regular (Round) Tip Version?

The FDA product code for Signia™ Small Diameter Reloads Including Regular (Round) Tip Version is GDW.

相关临床试验

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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。

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