FDA 510(k)

Synergy 平台，Synergy，Infinity，VersaHD

K号: K192242 · 2019-11-22

决定日期2019-11-22

产品代码IYE

咨询委员会RA

决定实质等同

器械摘要

Synergy Platform, Synergy, Infinity, VersaHD is the device name listed in this FDA 510(k) record. The listed applicant is Elekta Limited. It received FDA 510(k) clearance on 2019-11-22 under 510(k) number K192242. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Synergy Platform, Synergy, Infinity, VersaHD?

Synergy Platform, Synergy, Infinity, VersaHD is a medical device that received FDA 510(k) clearance on 2019-11-22. The listed applicant is Elekta Limited. The 510(k) number is K192242.

When did Synergy Platform, Synergy, Infinity, VersaHD receive FDA 510(k) clearance?

Synergy Platform, Synergy, Infinity, VersaHD received FDA 510(k) clearance on 2019-11-22, under 510(k) number K192242.

Who is the listed applicant for Synergy Platform, Synergy, Infinity, VersaHD?

The FDA 510(k) record lists Elekta Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Synergy Platform, Synergy, Infinity, VersaHD?

The FDA product code for Synergy Platform, Synergy, Infinity, VersaHD is IYE.

列明Elekta Limited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。

K210500Elekta Synergy, Elekta Harmony, Elekta Infinity, Versa HD K192482Elekta Unity K182076Elekta Unity

官方来源

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