KUBTEC X250

System, X-ray, Mobile

KUB TECHNOLOGIES, INC

The following data is part of a premarket notification filed by Kub Technologies, Inc with the FDA for Kubtec X250.

Pre-market Notification Details

Device IDK141539
510k NumberK141539
Device Name:KUBTEC X250
ClassificationSystem, X-ray, Mobile
Applicant KUB TECHNOLOGIES, INC 270 ROWE AVENUE, UNIT E Milford,  CT  06461
ContactVikram Butani
CorrespondentVikram Butani
KUB TECHNOLOGIES, INC 270 ROWE AVENUE, UNIT E Milford,  CT  06461
Product CodeIZL  
CFR Regulation Number892.1720 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2014-06-10
Decision Date2014-10-29

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
B619KUB2500 K141539 000

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