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FDA 510(k)

X射线平板探测器/护理视界3600RF

K号: K202995 · 2021-02-19

决定日期2021-02-19
产品代码MQB
咨询委员会RA
决定实质等同

器械摘要

X-ray Flat Panel Detectors/CareView 3600RF is the device name listed in this FDA 510(k) record. The listed applicant is Careray Digital Medical System Co., Ltd.. It received FDA 510(k) clearance on 2021-02-19 under 510(k) number K202995. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the X-ray Flat Panel Detectors/CareView 3600RF?

X-ray Flat Panel Detectors/CareView 3600RF is a medical device that received FDA 510(k) clearance on 2021-02-19. The listed applicant is Careray Digital Medical System Co., Ltd.. The 510(k) number is K202995.

When did X-ray Flat Panel Detectors/CareView 3600RF receive FDA 510(k) clearance?

X-ray Flat Panel Detectors/CareView 3600RF received FDA 510(k) clearance on 2021-02-19, under 510(k) number K202995.

Who is the listed applicant for X-ray Flat Panel Detectors/CareView 3600RF?

The FDA 510(k) record lists Careray Digital Medical System Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for X-ray Flat Panel Detectors/CareView 3600RF?

The FDA product code for X-ray Flat Panel Detectors/CareView 3600RF is MQB.

相关临床试验

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列明Careray Digital Medical System Co., Ltd.为申报人的其他记录

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相关器械(代码:MQB)

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。

官方来源

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