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FDA 510(k)

iQMR

K-Number: K173605 · 2018-03-08

ApplicantMedic Vision - Imaging Solutions, Ltd.
Decision Date2018-03-08
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

iQMR is a medical device manufactured by Medic Vision - Imaging Solutions, Ltd.. It received FDA 510(k) clearance on 2018-03-08 under approval number K173605. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the iQMR?

iQMR is a medical device that received FDA 510(k) clearance on 2018-03-08. It is manufactured by Medic Vision - Imaging Solutions, Ltd.. The 510(k) number is K173605.

When was iQMR approved by the FDA?

iQMR received FDA 510(k) clearance on 2018-03-08, under approval number K173605.

What company makes iQMR?

iQMR is manufactured by Medic Vision - Imaging Solutions, Ltd..

What is the FDA product code for iQMR?

The FDA product code for iQMR is LLZ.

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Official Source

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

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