Kubtec Mozart Supra

Cabinet, X-ray System

KUB Technologies, Inc.

The following data is part of a premarket notification filed by Kub Technologies, Inc. with the FDA for Kubtec Mozart Supra.

Pre-market Notification Details

Device IDK200756
510k NumberK200756
Device Name:Kubtec Mozart Supra
ClassificationCabinet, X-ray System
Applicant KUB Technologies, Inc. 111 Research Drive Stratford,  CT  06615
ContactChester Lowe
CorrespondentChester Lowe
KUB Technologies, Inc. 111 Research Drive Stratford,  CT  06615
Product CodeMWP  
CFR Regulation Number892.1680 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2020-03-24
Decision Date2020-06-12

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