FDA 510(k)

EchoS

K号: K180516 · 2018-10-19

决定日期2018-10-19

产品代码MUA

咨询委员会RA

决定实质等同

器械摘要

EchoS is the device name listed in this FDA 510(k) record. The listed applicant is Echolight S.P.A. It received FDA 510(k) clearance on 2018-10-19 under 510(k) number K180516. The device is classified under product code MUA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the EchoS?

EchoS is a medical device that received FDA 510(k) clearance on 2018-10-19. The listed applicant is Echolight S.P.A. The 510(k) number is K180516.

When did EchoS receive FDA 510(k) clearance?

EchoS received FDA 510(k) clearance on 2018-10-19, under 510(k) number K180516.

Who is the listed applicant for EchoS?

The FDA 510(k) record lists Echolight S.P.A as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EchoS?

The FDA product code for EchoS is MUA.

列明Echolight S.P.A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。

K212851EchoSK 和 EchoSGyn 模块，适用于 EchoS 家族设备 K202514EchoS 家族

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。