FDA 510(k)

EIDON FA

K号: K180526 · 2018-07-16

决定日期2018-07-16

产品代码MYC

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决定实质等同

器械摘要

EIDON FA is the device name listed in this FDA 510(k) record. The listed applicant is Centervue S.P.A.. It received FDA 510(k) clearance on 2018-07-16 under 510(k) number K180526. The device is classified under product code MYC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the EIDON FA?

EIDON FA is a medical device that received FDA 510(k) clearance on 2018-07-16. The listed applicant is Centervue S.P.A.. The 510(k) number is K180526.

When did EIDON FA receive FDA 510(k) clearance?

EIDON FA received FDA 510(k) clearance on 2018-07-16, under 510(k) number K180526.

Who is the listed applicant for EIDON FA?

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

What is the FDA product code for EIDON FA?

The FDA product code for EIDON FA is MYC.

列明Centervue 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。

K243504MAIA (AHMACME001)K234076iCare ALTIUS CW K213705DRSplus K211328EIDON FA，EIDON，EIDON AF，EIDON UWFL K192113DRSplus K180293Retia 2

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