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FDA 510(k)

Nexus DRTM 数字X射线成像系统(带PaxScan 4336Wv4)

K号: K161459 · 2016-09-06

决定日期2016-09-06
产品代码MQB
咨询委员会RA
决定实质等同

器械摘要

Nexus DRTM Digital X-ray Imaging System (with PaxScan 4336Wv4) is the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems, X-Ray Products-Infimed. It received FDA 510(k) clearance on 2016-09-06 under 510(k) number K161459. 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 Nexus DRTM Digital X-ray Imaging System (with PaxScan 4336Wv4)?

Nexus DRTM Digital X-ray Imaging System (with PaxScan 4336Wv4) is a medical device that received FDA 510(k) clearance on 2016-09-06. The listed applicant is Varian Medical Systems, X-Ray Products-Infimed. The 510(k) number is K161459.

When did Nexus DRTM Digital X-ray Imaging System (with PaxScan 4336Wv4) receive FDA 510(k) clearance?

Nexus DRTM Digital X-ray Imaging System (with PaxScan 4336Wv4) received FDA 510(k) clearance on 2016-09-06, under 510(k) number K161459.

Who is the listed applicant for Nexus DRTM Digital X-ray Imaging System (with PaxScan 4336Wv4)?

The FDA 510(k) record lists Varian Medical Systems, X-Ray Products-Infimed as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nexus DRTM Digital X-ray Imaging System (with PaxScan 4336Wv4)?

The FDA product code for Nexus DRTM Digital X-ray Imaging System (with PaxScan 4336Wv4) is MQB.

相关临床试验

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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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