Q-Switched Nd:YAG Laser System
K号: K171079 · 2017-08-01
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器械摘要
Q-Switched Nd:YAG Laser System is the device name listed in this FDA 510(k) record. The listed applicant is Ids, Ltd.. It received FDA 510(k) clearance on 2017-08-01 under 510(k) number K171079. 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 Q-Switched Nd:YAG Laser System?
Q-Switched Nd:YAG Laser System is a medical device that received FDA 510(k) clearance on 2017-08-01. The listed applicant is Ids, Ltd.. The 510(k) number is K171079.
When did Q-Switched Nd:YAG Laser System receive FDA 510(k) clearance?
Q-Switched Nd:YAG Laser System received FDA 510(k) clearance on 2017-08-01, under 510(k) number K171079.
Who is the listed applicant for Q-Switched Nd:YAG Laser System?
The FDA 510(k) record lists Ids, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Q-Switched Nd:YAG Laser System?
The FDA product code for Q-Switched Nd:YAG Laser System is GEX. This falls under the Gastroenterology category.
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列明Ids, Ltd.为申报人的其他记录
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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
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