Cutera enlighten III 激光系统
K号: K160488 · 2016-10-28
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器械摘要
Cutera enlighten III Laser System is the device name listed in this FDA 510(k) record. The listed applicant is Cutera, Inc.. It received FDA 510(k) clearance on 2016-10-28 under 510(k) number K160488. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.
常见问题
What is the Cutera enlighten III Laser System?
Cutera enlighten III Laser System is a medical device that received FDA 510(k) clearance on 2016-10-28. The listed applicant is Cutera, Inc.. The 510(k) number is K160488.
When did Cutera enlighten III Laser System receive FDA 510(k) clearance?
Cutera enlighten III Laser System received FDA 510(k) clearance on 2016-10-28, under 510(k) number K160488.
Who is the listed applicant for Cutera enlighten III Laser System?
The FDA 510(k) record lists Cutera, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cutera enlighten III Laser System?
The FDA product code for Cutera enlighten III Laser System is GEX. This falls under the Gastroenterology category.
相关临床试验
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列明Cutera, Inc.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：GEX）
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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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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