FDA 510(k)

ImagingRing 系统（轨道式）

K号: K191267 · 2019-08-01

决定日期2019-08-01

产品代码IYE

咨询委员会RA

决定实质等同

器械摘要

ImagingRing System on Rails is the device name listed in this FDA 510(k) record. The listed applicant is Medphoton GmbH. It received FDA 510(k) clearance on 2019-08-01 under 510(k) number K191267. 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 ImagingRing System on Rails?

ImagingRing System on Rails is a medical device that received FDA 510(k) clearance on 2019-08-01. The listed applicant is Medphoton GmbH. The 510(k) number is K191267.

When did ImagingRing System on Rails receive FDA 510(k) clearance?

ImagingRing System on Rails received FDA 510(k) clearance on 2019-08-01, under 510(k) number K191267.

Who is the listed applicant for ImagingRing System on Rails?

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

What is the FDA product code for ImagingRing System on Rails?

The FDA product code for ImagingRing System on Rails is IYE.

列明Medphoton GmbH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。

K234067ImagingRing m（版本2.0）；Loop-X（版本2.0）；Loop-X 移动成像机器人（版本2.0）K203281Mobile ImagingRing 系统，IRm，Loop-X 移动成像机器人，Loop-X K161400ImagingRing 系统

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。