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 the device name listed in this FDA 510(k) record. The listed applicant is Medic Vision - Imaging Solutions, Ltd.. It received FDA 510(k) clearance on 2018-03-08 under 510(k) 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. The listed applicant is Medic Vision - Imaging Solutions, Ltd.. The 510(k) number is K173605.

When did iQMR receive FDA 510(k) clearance?

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

Who is the listed applicant for iQMR?

The FDA 510(k) record lists Medic Vision - Imaging Solutions, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for iQMR?

The FDA product code for iQMR is LLZ.

Other records listing Medic Vision - Imaging Solutions, Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.