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FDA 510(k)

电外科手术发生器(ES-100);电外科手术发生器(ES-300)

K号: K240975 · 2024-12-23

决定日期2024-12-23
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

Electrosurgical Generator (ES-100); Electrosurgical Generator (ES-300) is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Taktvoll Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-12-23 under 510(k) number K240975. 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 Electrosurgical Generator (ES-100); Electrosurgical Generator (ES-300)?

Electrosurgical Generator (ES-100); Electrosurgical Generator (ES-300) is a medical device that received FDA 510(k) clearance on 2024-12-23. The listed applicant is Beijing Taktvoll Technology Co., Ltd.. The 510(k) number is K240975.

When did Electrosurgical Generator (ES-100); Electrosurgical Generator (ES-300) receive FDA 510(k) clearance?

Electrosurgical Generator (ES-100); Electrosurgical Generator (ES-300) received FDA 510(k) clearance on 2024-12-23, under 510(k) number K240975.

Who is the listed applicant for Electrosurgical Generator (ES-100); Electrosurgical Generator (ES-300)?

The FDA 510(k) record lists Beijing Taktvoll Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Electrosurgical Generator (ES-100); Electrosurgical Generator (ES-300)?

The FDA product code for Electrosurgical Generator (ES-100); Electrosurgical Generator (ES-300) is GEI.

相关临床试验

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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。

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