FDA 510(k)ProSun 太阳灯产品,Luxura 太阳灯产品
K号: K181455 · 2018-09-10
决定日期2018-09-10
产品代码LEJ
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
ProSun sunlamp products, Luxura sunlamp products is the device name listed in this FDA 510(k) record. The listed applicant is Prosun International, LLC. It received FDA 510(k) clearance on 2018-09-10 under 510(k) number K181455. The device is classified under product code LEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the ProSun sunlamp products, Luxura sunlamp products?
ProSun sunlamp products, Luxura sunlamp products is a medical device that received FDA 510(k) clearance on 2018-09-10. The listed applicant is Prosun International, LLC. The 510(k) number is K181455.
When did ProSun sunlamp products, Luxura sunlamp products receive FDA 510(k) clearance?
ProSun sunlamp products, Luxura sunlamp products received FDA 510(k) clearance on 2018-09-10, under 510(k) number K181455.
Who is the listed applicant for ProSun sunlamp products, Luxura sunlamp products?
The FDA 510(k) record lists Prosun International, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ProSun sunlamp products, Luxura sunlamp products?
The FDA product code for ProSun sunlamp products, Luxura sunlamp products is LEJ.
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相关器械(代码:LEJ)
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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