FDA 510(k)

x-mind dc（商标名下为Acteon），Owandy-RX DC（商标名下为OwandyRadiology）

K号: K231055 · 2023-12-28

决定日期2023-12-28

产品代码EHD

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决定实质等同

器械摘要

x-mind dc (under trademark Acteon), Owandy-RX DC (under trademark OwandyRadiology) is the device name listed in this FDA 510(k) record. The listed applicant is De Götzen S.R.L.. It received FDA 510(k) clearance on 2023-12-28 under 510(k) number K231055. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the x-mind dc (under trademark Acteon), Owandy-RX DC (under trademark OwandyRadiology)?

x-mind dc (under trademark Acteon), Owandy-RX DC (under trademark OwandyRadiology) is a medical device that received FDA 510(k) clearance on 2023-12-28. The listed applicant is De Götzen S.R.L.. The 510(k) number is K231055.

When did x-mind dc (under trademark Acteon), Owandy-RX DC (under trademark OwandyRadiology) receive FDA 510(k) clearance?

x-mind dc (under trademark Acteon), Owandy-RX DC (under trademark OwandyRadiology) received FDA 510(k) clearance on 2023-12-28, under 510(k) number K231055.

Who is the listed applicant for x-mind dc (under trademark Acteon), Owandy-RX DC (under trademark OwandyRadiology)?

The FDA 510(k) record lists De Götzen S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for x-mind dc (under trademark Acteon), Owandy-RX DC (under trademark OwandyRadiology)?

The FDA product code for x-mind dc (under trademark Acteon), Owandy-RX DC (under trademark OwandyRadiology) is EHD.

列明De Götzen 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。

K203374X-MIND prime（商标名下为Acteon），I-MAX（商标名下为Owandy Radiology）

官方来源

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