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FDA 510(k)

ArtPIX DRF

K-Number: K202235 · 2020-09-03

ApplicantCmt Medical Technologies, Ltd.
Decision Date2020-09-03
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ArtPIX DRF is a medical device manufactured by Cmt Medical Technologies, Ltd.. It received FDA 510(k) clearance on 2020-09-03 under approval number K202235. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ArtPIX DRF?

ArtPIX DRF is a medical device that received FDA 510(k) clearance on 2020-09-03. It is manufactured by Cmt Medical Technologies, Ltd.. The 510(k) number is K202235.

When was ArtPIX DRF approved by the FDA?

ArtPIX DRF received FDA 510(k) clearance on 2020-09-03, under approval number K202235.

What company makes ArtPIX DRF?

ArtPIX DRF is manufactured by Cmt Medical Technologies, Ltd..

What is the FDA product code for ArtPIX DRF?

The FDA product code for ArtPIX DRF is JAA.

Other Devices by Cmt Medical Technologies, Ltd.

K162224ArtPix Mobile EZ2GO

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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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