Soli-Lite LG4 Galileo
K号: K192755 · 2019-12-20
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决定日期2019-12-20
产品代码GEX
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
Soli-Lite LG4 Galileo is the device name listed in this FDA 510(k) record. The listed applicant is Silhouet-Tone Corporation. It received FDA 510(k) clearance on 2019-12-20 under 510(k) number K192755. 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 Soli-Lite LG4 Galileo?
Soli-Lite LG4 Galileo is a medical device that received FDA 510(k) clearance on 2019-12-20. The listed applicant is Silhouet-Tone Corporation. The 510(k) number is K192755.
When did Soli-Lite LG4 Galileo receive FDA 510(k) clearance?
Soli-Lite LG4 Galileo received FDA 510(k) clearance on 2019-12-20, under 510(k) number K192755.
Who is the listed applicant for Soli-Lite LG4 Galileo?
The FDA 510(k) record lists Silhouet-Tone Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Soli-Lite LG4 Galileo?
The FDA product code for Soli-Lite LG4 Galileo is GEX. This falls under the Gastroenterology category.
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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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