FDA 510(k)

LaVid FMTS 诊断 X 射线系统

K号: K180663 · 2018-05-18

决定日期2018-05-18

产品代码KPR

咨询委员会RA

决定实质等同

器械摘要

LaVid FMTS DIAGNOSTIC X-RAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Livermoretech, Inc.. It received FDA 510(k) clearance on 2018-05-18 under 510(k) number K180663. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the LaVid FMTS DIAGNOSTIC X-RAY SYSTEM?

LaVid FMTS DIAGNOSTIC X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 2018-05-18. The listed applicant is Livermoretech, Inc.. The 510(k) number is K180663.

When did LaVid FMTS DIAGNOSTIC X-RAY SYSTEM receive FDA 510(k) clearance?

LaVid FMTS DIAGNOSTIC X-RAY SYSTEM received FDA 510(k) clearance on 2018-05-18, under 510(k) number K180663.

Who is the listed applicant for LaVid FMTS DIAGNOSTIC X-RAY SYSTEM?

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

What is the FDA product code for LaVid FMTS DIAGNOSTIC X-RAY SYSTEM?

The FDA product code for LaVid FMTS DIAGNOSTIC X-RAY SYSTEM is KPR.

列明Livermoretech, Inc.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。

K244049Europa（备选：AiRTouch）便携式X射线系统 K193535EZER，便携式 X 射线系统 K200022FLUSION-9001, Fluoroscopic C-arm Mobile X-ray System K193644E-COM DR-2000 DR K190935EZER，便携式 X 射线系统

官方来源

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