FDA 510(k)

Eusol-C

K号: K162013 · 2016-09-15

决定日期2016-09-15

产品代码LYX

决定实质等同

器械摘要

Eusol-C is the device name listed in this FDA 510(k) record. The listed applicant is Al.Chi.Mi.A. S.R.L. It received FDA 510(k) clearance on 2016-09-15 under 510(k) number K162013. The device is classified under product code LYX. FDA Decision: Substantially Equivalent.

常见问题

What is the Eusol-C?

Eusol-C is a medical device that received FDA 510(k) clearance on 2016-09-15. The listed applicant is Al.Chi.Mi.A. S.R.L. The 510(k) number is K162013.

When did Eusol-C receive FDA 510(k) clearance?

Eusol-C received FDA 510(k) clearance on 2016-09-15, under 510(k) number K162013.

Who is the listed applicant for Eusol-C?

The FDA 510(k) record lists Al.Chi.Mi.A. S.R.L as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Eusol-C?

The FDA product code for Eusol-C is LYX.

列明Al.Chi.Mi.A. S.R.L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。

K251320XTRA4

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。