FDA 510(k)

Aquarius 8600 1417WCI; Aquarius 8600 1717WCI

K号: K173273 · 2017-11-09

决定日期2017-11-09

产品代码MQB

咨询委员会RA

决定实质等同

器械摘要

Aquarius 8600 1417WCI; Aquarius 8600 1717WCI 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 2017-11-09 under 510(k) number K173273. 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 1417WCI; Aquarius 8600 1717WCI?

Aquarius 8600 1417WCI; Aquarius 8600 1717WCI is a medical device that received FDA 510(k) clearance on 2017-11-09. The listed applicant is Imaging Dynamics Company , Ltd.. The 510(k) number is K173273.

When did Aquarius 8600 1417WCI; Aquarius 8600 1717WCI receive FDA 510(k) clearance?

Aquarius 8600 1417WCI; Aquarius 8600 1717WCI received FDA 510(k) clearance on 2017-11-09, under 510(k) number K173273.

Who is the listed applicant for Aquarius 8600 1417WCI; Aquarius 8600 1717WCI?

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 1417WCI; Aquarius 8600 1717WCI?

The FDA product code for Aquarius 8600 1417WCI; Aquarius 8600 1717WCI 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。

K171169Aquarius 8600 1417TG 和 Aquarius 8600 1717TG K171175Aquarius 8600 1417WC K170202Aquarius 8600

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