GXR-Series Diagnostic X-Ray System

System, X-ray, Stationary

DRGEM Corporation

The following data is part of a premarket notification filed by Drgem Corporation with the FDA for Gxr-series Diagnostic X-ray System.

Pre-market Notification Details

Device IDK202572
510k NumberK202572
Device Name:GXR-Series Diagnostic X-Ray System
ClassificationSystem, X-ray, Stationary
Applicant DRGEM Corporation 7F E-B/D Gwangmyeong Techno-Park 60, Haan-ro Gwangmyeong-si,  KR 14322
ContactKi-nam Yang
CorrespondentCarl Alletto
OTech Inc. 8317 Belew Drive Mckinney,  TX  75071
Product CodeKPR  
CFR Regulation Number892.1680 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2020-09-04
Decision Date2020-09-24

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