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FDA 510(k)

Aquarius 8600 1417WCI; Aquarius 8600 1717WCI

K-Number: K173273 · 2017-11-09

ApplicantImaging Dynamics Company , Ltd.
Decision Date2017-11-09
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Aquarius 8600 1417WCI; Aquarius 8600 1717WCI is a medical device manufactured by Imaging Dynamics Company , Ltd.. It received FDA 510(k) clearance on 2017-11-09 under approval number K173273. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

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. It is manufactured by Imaging Dynamics Company , Ltd.. The 510(k) number is K173273.

When was Aquarius 8600 1417WCI; Aquarius 8600 1717WCI approved by the FDA?

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

What company makes Aquarius 8600 1417WCI; Aquarius 8600 1717WCI?

Aquarius 8600 1417WCI; Aquarius 8600 1717WCI is manufactured by Imaging Dynamics Company , Ltd..

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.

Other Devices by Imaging Dynamics Company , Ltd.

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

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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