FDA 510(k) Applications Submitted by JAE KIM
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K130088 |
01/14/2013 |
PORT VIEW, DIGITAL X-RAY SENSOR SYSTEM |
GENORAY CO., LTD. |
K120263 |
01/30/2012 |
VOLUX 21C, DIGITAL EXTRAORAL SOURCE X-RAY SYSTEM |
GENORAY CO., LTD. |
K130419 |
02/19/2013 |
PAPAYA PLUS, DIGITAL EXTRAORAL SOURCE X-RAY SYSTEM |
GENORAY CO., LTD. |
K092171 |
07/21/2009 |
VOLUX, DIGITAL EXTRAORAL SOURCE X-RAY SYSTEM |
GENORAY CO., LTD. |
K103181 |
10/28/2010 |
ZENIS, PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM |
GENORAY CO., LTD. |
K103182 |
10/28/2010 |
TRIANA, PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM |
GENORAY CO., LTD. |
K103425 |
11/22/2010 |
ZEN-7000, FLUOROSCOPIC X-RAY SYSTEM |
GENORAY AMERICA INC. |
K200022 |
01/06/2020 |
FLUSION-9001, Fluoroscopic C-arm Mobile X-ray System |
LiverMoreTech Inc. |
K180663 |
03/14/2018 |
LaVid FMTS DIAGNOSTIC X-RAY SYSTEM |
LIVERMORETECH Inc. |
K190935 |
04/10/2019 |
EZER, Portable X-ray System |
Livermoretech Inc. |
K193535 |
12/20/2019 |
EZER, Portable X-ray System |
Livermoretech Inc. |
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