CuRAS Nd:YAG 激光
K号: K173038 · 2017-12-01
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器械摘要
CuRAS Nd:YAG Laser is the device name listed in this FDA 510(k) record. The listed applicant is Ilooda Co,., Ltd.. It received FDA 510(k) clearance on 2017-12-01 under 510(k) number K173038. 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 CuRAS Nd:YAG Laser?
CuRAS Nd:YAG Laser is a medical device that received FDA 510(k) clearance on 2017-12-01. The listed applicant is Ilooda Co,., Ltd.. The 510(k) number is K173038.
When did CuRAS Nd:YAG Laser receive FDA 510(k) clearance?
CuRAS Nd:YAG Laser received FDA 510(k) clearance on 2017-12-01, under 510(k) number K173038.
Who is the listed applicant for CuRAS Nd:YAG Laser?
The FDA 510(k) record lists Ilooda Co,., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CuRAS Nd:YAG Laser?
The FDA product code for CuRAS Nd:YAG Laser is GEX. This falls under the Gastroenterology category.
相关临床试验
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列明Ilooda Co,., 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：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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