UPnRIDE
K号: K182257 · 2019-09-12
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决定日期2019-09-12
产品代码IPL
咨询委员会PM
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器械摘要
UPnRIDE is the device name listed in this FDA 510(k) record. The listed applicant is Upnride Robotics , Ltd.. It received FDA 510(k) clearance on 2019-09-12 under 510(k) number K182257. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the UPnRIDE?
UPnRIDE is a medical device that received FDA 510(k) clearance on 2019-09-12. The listed applicant is Upnride Robotics , Ltd.. The 510(k) number is K182257.
When did UPnRIDE receive FDA 510(k) clearance?
UPnRIDE received FDA 510(k) clearance on 2019-09-12, under 510(k) number K182257.
Who is the listed applicant for UPnRIDE?
The FDA 510(k) record lists Upnride Robotics , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UPnRIDE?
The FDA product code for UPnRIDE is IPL.
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相关器械（代码：IPL）
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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