FDA 510(k) Applications Submitted by CMT MEDICAL TECHNOLOGIES, LTD.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K080890 |
03/31/2008 |
SMARTSPOT PRIMAX |
CMT MEDICAL TECHNOLOGIES, LTD. |
| K001111 |
04/06/2000 |
PANORET, MODEL 1000A |
CMT MEDICAL TECHNOLOGIES, LTD. |
| K961140 |
03/21/1996 |
FLUOROPLUS CARDIAC TV |
CMT MEDICAL TECHNOLOGIES, LTD. |
| K961307 |
04/04/1996 |
SMART SPOT |
CMT MEDICAL TECHNOLOGIES, LTD. |
| K162224 |
08/08/2016 |
ArtPix Mobile EZ2GO |
CMT MEDICAL TECHNOLOGIES, LTD. |
| K100400 |
02/16/2010 |
PRESTODR PORTABLE |
CMT MEDICAL TECHNOLOGIES, LTD. |
| K110849 |
03/28/2011 |
PRESTODR 4143 |
CMT MEDICAL TECHNOLOGIES, LTD. |
| K103038 |
10/14/2010 |
DUET DRF |
CMT MEDICAL TECHNOLOGIES, LTD. |
| K991578 |
05/06/1999 |
SMARTSPOT 2000 |
CMT MEDICAL TECHNOLOGIES, LTD. |
| K003438 |
11/06/2000 |
SMART RAD |
CMT MEDICAL TECHNOLOGIES, LTD. |
|
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