Ep Medsystems
FDA 510(k) & PMA Approved Devices — 12 products
Advertisement
Total Devices12
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K092913 | EP-4TM CARDIAC STIMULATOR, MODELS: EP-04-02, EP-04-04 | JOQ | 2009-10-16 | View |
| 510(k) | K073709 | MODIFICATION TO VIEWMATE SYSTEM | IYN | 2008-03-11 | View |
| 510(k) | K071028 | VIEWMATE SYSTEM | ITN | 2007-05-01 | View |
| 510(k) | K070706 | EP-WORKMATE | DQK | 2007-04-11 | View |
| 510(k) | K063113 | EP-WORKMATE | DQK | 2006-10-27 | View |
| 510(k) | K041442 | EP-4 CLINICAL STIMUTATOR | JOQ | 2004-09-14 | View |
| 510(k) | K040207 | EP-4 CLINICAL STIMULATOR | JOQ | 2004-02-27 | View |
| 510(k) | K031066 | VIEWMATE ULTRASOUND IMAGING SYSTEM | IYN | 2003-10-17 | View |
| 510(k) | K032225 | EP-WORKMATE WITH RPM SYSTEM | DQK | 2003-08-20 | View |
| 510(k) | K991001 | MODIFICATION OF PROCATH ELECTROPHYSIOLOGY CATHETER, EP MEDSYSTEMS ELECTROPHYSIOLOGY CATHETER | DRF | 1999-07-15 | View |
| 510(k) | K984150 | PROCATH ELECTROPHYSIOLOGY CATHETER, EP MEDSYSTEMS ELECTROPHYSIOLOGY CATHETER | DRF | 1999-02-22 | View |
| 510(k) | K961513 | PROCATH LOCKING PEEL-AWAY INTRODUCER/PEEL-AWAY INTRODUCER SET | DYB | 1996-05-13 | View |
No matching devices.
Advertisement