Aquarius 8600 1417TG and Aquarius 8600 1717TG
K-Number: K171169 · 2017-10-12
ApplicantImaging Dynamics Company , Ltd.
Decision Date2017-10-12
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Aquarius 8600 1417TG and Aquarius 8600 1717TG is a medical device manufactured by Imaging Dynamics Company , Ltd.. It received FDA 510(k) clearance on 2017-10-12 under approval number K171169. 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 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. It is manufactured by Imaging Dynamics Company , Ltd.. The 510(k) number is K171169.
When was Aquarius 8600 1417TG and Aquarius 8600 1717TG approved by the FDA?
Aquarius 8600 1417TG and Aquarius 8600 1717TG received FDA 510(k) clearance on 2017-10-12, under approval number K171169.
What company makes Aquarius 8600 1417TG and Aquarius 8600 1717TG?
Aquarius 8600 1417TG and Aquarius 8600 1717TG is manufactured by Imaging Dynamics Company , Ltd..
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.
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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.