Creo Medical Electrosurgical System including Speedboat RS2 Surgical Accessory
K号: K171983 · 2017-08-17
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器械摘要
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。
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
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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