The following data is part of a premarket notification filed by Drgem Corporation with the FDA for Gxr-series Diagnostic X-ray System.
Device ID | K192364 |
510k Number | K192364 |
Device Name: | GXR-Series Diagnostic X-Ray System |
Classification | System, X-ray, Stationary |
Applicant | DRGEM Corporation 7F E-B/D Gwangmyeong Techno-Park 60, Haan-ro Gwangmyeong-si, KR 14322 |
Contact | Ki-nam Yang |
Correspondent | Carl Aletto OTech Inc. 8317 Belew Drive Mckinney, TX 75071 |
Product Code | KPR |
CFR Regulation Number | 892.1680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-08-30 |
Decision Date | 2019-09-26 |
Summary: | summary |