MX40 版本 B.07
K号: K172226 · 2017-11-09
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器械摘要
常见问题
What is the MX40 Release B.07?
MX40 Release B.07 is a medical device that received FDA 510(k) clearance on 2017-11-09. The listed applicant is Philips Medical Systems. The 510(k) number is K172226.
When did MX40 Release B.07 receive FDA 510(k) clearance?
MX40 Release B.07 received FDA 510(k) clearance on 2017-11-09, under 510(k) number K172226.
Who is the listed applicant for MX40 Release B.07?
The FDA 510(k) record lists Philips Medical Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MX40 Release B.07?
The FDA product code for MX40 Release B.07 is MHX.
相关临床试验
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。
列明Philips Medical Systems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:MHX)
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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