FDA 510(k)

Kubtec Mozart (Xpert42)

K-Number: K183624 · 2019-06-20

Decision Date2019-06-20

Product CodeMWP

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Kubtec Mozart (Xpert42) is a medical device manufactured by Kub Technologies, Inc.. It received FDA 510(k) clearance on 2019-06-20 under approval number K183624. The device is classified under product code MWP. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Kubtec Mozart (Xpert42)?

Kubtec Mozart (Xpert42) is a medical device that received FDA 510(k) clearance on 2019-06-20. It is manufactured by Kub Technologies, Inc.. The 510(k) number is K183624.

When was Kubtec Mozart (Xpert42) approved by the FDA?

Kubtec Mozart (Xpert42) received FDA 510(k) clearance on 2019-06-20, under approval number K183624.

What company makes Kubtec Mozart (Xpert42)?

Kubtec Mozart (Xpert42) is manufactured by Kub Technologies, Inc..

What is the FDA product code for Kubtec Mozart (Xpert42)?

The FDA product code for Kubtec Mozart (Xpert42) is MWP.

Other Devices by Kub Technologies, Inc.

K200756Kubtec Mozart Supra K210955Kubtec Mozart Supra (XPERT 84) Radiography System K210956Kubtec Mozart (XPERT42) K210957Kubec Xpert 80 Radiography System

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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.