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FDA 510(k)

ArtPix Mobile EZ2GO

K-Number: K162224 · 2016-09-22

ApplicantCmt Medical Technologies, Ltd.
Decision Date2016-09-22
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ArtPix Mobile EZ2GO is a medical device manufactured by Cmt Medical Technologies, Ltd.. It received FDA 510(k) clearance on 2016-09-22 under approval number K162224. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ArtPix Mobile EZ2GO?

ArtPix Mobile EZ2GO is a medical device that received FDA 510(k) clearance on 2016-09-22. It is manufactured by Cmt Medical Technologies, Ltd.. The 510(k) number is K162224.

When was ArtPix Mobile EZ2GO approved by the FDA?

ArtPix Mobile EZ2GO received FDA 510(k) clearance on 2016-09-22, under approval number K162224.

What company makes ArtPix Mobile EZ2GO?

ArtPix Mobile EZ2GO is manufactured by Cmt Medical Technologies, Ltd..

What is the FDA product code for ArtPix Mobile EZ2GO?

The FDA product code for ArtPix Mobile EZ2GO is KPR.

Other Devices by Cmt Medical Technologies, Ltd.

K202235ArtPIX DRF

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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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