FDA 510(k)

Aquarius 8600 1417TG 和 Aquarius 8600 1717TG

K号: K171169 · 2017-10-12

决定日期2017-10-12

产品代码MQB

咨询委员会RA

决定实质等同

器械摘要

Aquarius 8600 1417TG and Aquarius 8600 1717TG is the device name listed in this FDA 510(k) record. The listed applicant is Imaging Dynamics Company , Ltd.. It received FDA 510(k) clearance on 2017-10-12 under 510(k) number K171169. 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 Aquarius 8600 1417TG and Aquarius 8600 1717TG?

Aquarius 8600 1417TG and Aquarius 8600 1717TG is a medical device that received FDA 510(k) clearance on 2017-10-12. The listed applicant is Imaging Dynamics Company , Ltd.. The 510(k) number is K171169.

When did Aquarius 8600 1417TG and Aquarius 8600 1717TG receive FDA 510(k) clearance?

Aquarius 8600 1417TG and Aquarius 8600 1717TG received FDA 510(k) clearance on 2017-10-12, under 510(k) number K171169.

Who is the listed applicant for Aquarius 8600 1417TG and Aquarius 8600 1717TG?

The FDA 510(k) record lists Imaging Dynamics Company , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Aquarius 8600 1417TG and Aquarius 8600 1717TG?

The FDA product code for Aquarius 8600 1417TG and Aquarius 8600 1717TG is MQB.

列明Imaging Dynamics Company , Ltd.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。

K173273Aquarius 8600 1417WCI; Aquarius 8600 1717WCI K171175Aquarius 8600 1417WC K170202Aquarius 8600

官方来源

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