MU2net
K号: K191944 · 2019-10-24
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器械摘要
MU2net is the device name listed in this FDA 510(k) record. The listed applicant is Dosisoft. It received FDA 510(k) clearance on 2019-10-24 under 510(k) number K191944. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MU2net?
MU2net is a medical device that received FDA 510(k) clearance on 2019-10-24. The listed applicant is Dosisoft. The 510(k) number is K191944.
When did MU2net receive FDA 510(k) clearance?
MU2net received FDA 510(k) clearance on 2019-10-24, under 510(k) number K191944.
Who is the listed applicant for MU2net?
The FDA 510(k) record lists Dosisoft as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MU2net?
The FDA product code for MU2net is IYE.
列明Dosisoft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：IYE）
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。
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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