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FDA 510(k)

Creo Medical Electrosurgical System including Speedboat RS2 Surgical Accessory

K号: K171983 · 2017-08-17

决定日期2017-08-17
产品代码KNS
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。
决定实质等同

器械摘要

Creo Medical Electrosurgical System including Speedboat RS2 Surgical Accessory is the device name listed in this FDA 510(k) record. The listed applicant is Creo Medical, Ltd.. It received FDA 510(k) clearance on 2017-08-17 under 510(k) number K171983. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Creo Medical Electrosurgical System including Speedboat RS2 Surgical Accessory?

Creo Medical Electrosurgical System including Speedboat RS2 Surgical Accessory is a medical device that received FDA 510(k) clearance on 2017-08-17. The listed applicant is Creo Medical, Ltd.. The 510(k) number is K171983.

When did Creo Medical Electrosurgical System including Speedboat RS2 Surgical Accessory receive FDA 510(k) clearance?

Creo Medical Electrosurgical System including Speedboat RS2 Surgical Accessory received FDA 510(k) clearance on 2017-08-17, under 510(k) number K171983.

Who is the listed applicant for Creo Medical Electrosurgical System including Speedboat RS2 Surgical Accessory?

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

What is the FDA product code for Creo Medical Electrosurgical System including Speedboat RS2 Surgical Accessory?

The FDA product code for Creo Medical Electrosurgical System including Speedboat RS2 Surgical Accessory is KNS.

相关临床试验

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列明Creo Medical, Ltd.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。

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相关器械(代码:KNS)

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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