C015
K号: K192182 · 2020-01-17
广告
器械摘要
C015 is the device name listed in this FDA 510(k) record. The listed applicant is Micronica Srl. It received FDA 510(k) clearance on 2020-01-17 under 510(k) number K192182. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the C015?
C015 is a medical device that received FDA 510(k) clearance on 2020-01-17. The listed applicant is Micronica Srl. The 510(k) number is K192182.
When did C015 receive FDA 510(k) clearance?
C015 received FDA 510(k) clearance on 2020-01-17, under 510(k) number K192182.
Who is the listed applicant for C015?
The FDA 510(k) record lists Micronica Srl as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for C015?
The FDA product code for C015 is OWB.
相关器械(代码:OWB)
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。
广告