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FDA 510(k)

ArtPix Mobile EZ2GO

K-Number: K162224 · 2016-09-22

Decision Date2016-09-22
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ArtPix Mobile EZ2GO is the device name listed in this FDA 510(k) record. The listed applicant is Cmt Medical Technologies, Ltd.. It received FDA 510(k) clearance on 2016-09-22 under 510(k) 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. The listed applicant is Cmt Medical Technologies, Ltd.. The 510(k) number is K162224.

When did ArtPix Mobile EZ2GO receive FDA 510(k) clearance?

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

Who is the listed applicant for ArtPix Mobile EZ2GO?

The FDA 510(k) record lists Cmt Medical Technologies, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ArtPix Mobile EZ2GO?

The FDA product code for ArtPix Mobile EZ2GO is KPR.

Other records listing Cmt Medical Technologies, 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.

Related Devices (Code: KPR)

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.

Official Source

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