510(k) K210955

Kubtec Mozart Supra (XPERT 84) Radiography System by Kub Technologies, Inc. — Product Code MWP

K210955 is an FDA 510(k) premarket notification submitted by Kub Technologies, Inc. for the device "Kubtec Mozart Supra (XPERT 84) Radiography System". The FDA issued a decision of Substantially Equivalent on September 20, 2021. The device falls under product code MWP (Cabinet, X-Ray System), a Class II device regulated under 21 CFR 892.1680. Kub Technologies, Inc. has at least 9 other 510(k) clearances on record.