FDA 510(k) Applications Submitted by SHIN KUK YOO
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K120464 |
02/15/2012 |
INNESIS PEEK CAGE |
BK MEDITECH CO., LTD. |
| K091679 |
06/09/2009 |
LEFORTE SYSTEM BONE PLATE |
JEIL MEDICAL CORPORATION |
| K091686 |
06/09/2009 |
LEFORTE NEUROSYSTEM BONE SCREW |
JEIL MEDICAL CORPORATION |
| K111941 |
07/08/2011 |
CHOYANG THERMAL MASSAGER |
CHOYANG MEDICAL INSTRUMENT CO., LTD. |
| K082167 |
07/31/2008 |
PORTABLE X-RAY SYSTEM, MODELS DIOX-602, PROX |
DIGIMED CORPORATION |
| K092772 |
09/09/2009 |
PORTABLE X-RAY SYSTEM, MODEL HAND-RAY |
HANJIN DIGI-X CO., LTD. |
| K123476 |
11/13/2012 |
MEGA 5.5 SPINE SYSTEM |
LSK BIOPARTNERS, INC. |
| K091918 |
06/30/2009 |
ZEN-2090 PRO, FLUOROSCOPIC X-RAY SYSTEM, MODEL ZEN-2090 PRO |
GENORAY CO., LTD. |
| K082875 |
09/29/2008 |
PORTABLE X-RAY SYSTEM, MODEL DXR -1 |
EXARO CO., LTD. |
| K112992 |
10/06/2011 |
EARLOGIC OAE TESTER |
EARLOGIC CORPORATION |
|
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