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FDA 510(k)

Capenergy C Equipment RF System - C25, C50, C100, C200, C300, C400, C500

K号: K222260 · 2023-03-28

决定日期2023-03-28
产品代码PBX
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决定实质等同

器械摘要

Capenergy C Equipment RF System - C25, C50, C100, C200, C300, C400, C500 is the device name listed in this FDA 510(k) record. The listed applicant is Capenergy Medical S.L.. It received FDA 510(k) clearance on 2023-03-28 under 510(k) number K222260. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Capenergy C Equipment RF System - C25, C50, C100, C200, C300, C400, C500?

Capenergy C Equipment RF System - C25, C50, C100, C200, C300, C400, C500 is a medical device that received FDA 510(k) clearance on 2023-03-28. The listed applicant is Capenergy Medical S.L.. The 510(k) number is K222260.

When did Capenergy C Equipment RF System - C25, C50, C100, C200, C300, C400, C500 receive FDA 510(k) clearance?

Capenergy C Equipment RF System - C25, C50, C100, C200, C300, C400, C500 received FDA 510(k) clearance on 2023-03-28, under 510(k) number K222260.

Who is the listed applicant for Capenergy C Equipment RF System - C25, C50, C100, C200, C300, C400, C500?

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

What is the FDA product code for Capenergy C Equipment RF System - C25, C50, C100, C200, C300, C400, C500?

The FDA product code for Capenergy C Equipment RF System - C25, C50, C100, C200, C300, C400, C500 is PBX.

相关临床试验

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。

列明Capenergy Medical S.L.为申报人的其他记录

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。

相关器械(代码:PBX)

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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