FDA 510(k)

Kubtec Mozart Supra

K-Number: K200756 · 2020-06-12

Decision Date2020-06-12

Product CodeMWP

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Kubtec Mozart Supra is a medical device manufactured by Kub Technologies, Inc.. It received FDA 510(k) clearance on 2020-06-12 under approval number K200756. 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 Supra?

Kubtec Mozart Supra is a medical device that received FDA 510(k) clearance on 2020-06-12. It is manufactured by Kub Technologies, Inc.. The 510(k) number is K200756.

When was Kubtec Mozart Supra approved by the FDA?

Kubtec Mozart Supra received FDA 510(k) clearance on 2020-06-12, under approval number K200756.

What company makes Kubtec Mozart Supra?

Kubtec Mozart Supra is manufactured by Kub Technologies, Inc..

What is the FDA product code for Kubtec Mozart Supra?

The FDA product code for Kubtec Mozart Supra is MWP.

Other Devices by Kub Technologies, Inc.

K183624Kubtec Mozart (Xpert42) K210955Kubtec Mozart Supra (XPERT 84) Radiography System K210956Kubtec Mozart (XPERT42) K210957Kubec Xpert 80 Radiography System

Related Devices (Code: MWP)

K153583BioVision PlusFaxitron Bioptics, LLC K170786Faxitron Bioptics Speciemen Radiography SystemFaxitron Bioptics, LLC K173309Faxitron VisionCTFaxitron Bioptics, LLC K192939Volumetric Specimen ImagerClarix Imaging K193317CoreLite X-Ray Specimen CabinetCirdan Imaging Limited K183624Kubtec Mozart (Xpert42)Kub Technologies, Inc.

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.