Ep Medsystems - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Ep Medsystems has 12 FDA 510(k) cleared cardiovascular devices. Based in West Berlin, US.
Historical record: 12 cleared submissions from 1996 to 2009.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
12 devices
Cleared
Oct 16, 2009
EP-4TM CARDIAC STIMULATOR, MODELS: EP-04-02, EP-04-04
Cardiovascular
24d
Cleared
Mar 11, 2008
MODIFICATION TO VIEWMATE SYSTEM
Radiology
71d
Cleared
May 01, 2007
VIEWMATE SYSTEM
Radiology
20d
Cleared
Apr 11, 2007
EP-WORKMATE
Cardiovascular
28d
Cleared
Oct 27, 2006
EP-WORKMATE
Cardiovascular
16d
Cleared
Sep 14, 2004
EP-4 CLINICAL STIMUTATOR
Cardiovascular
105d
Cleared
Feb 27, 2004
EP-4 CLINICAL STIMULATOR
Cardiovascular
28d
Cleared
Oct 17, 2003
VIEWMATE ULTRASOUND IMAGING SYSTEM
Radiology
197d
Cleared
Aug 20, 2003
EP-WORKMATE WITH RPM SYSTEM
Cardiovascular
30d
Cleared
Jul 15, 1999
MODIFICATION OF PROCATH ELECTROPHYSIOLOGY CATHETER, EP MEDSYSTEMS...
Cardiovascular
112d
Cleared
Feb 22, 1999
PROCATH ELECTROPHYSIOLOGY CATHETER, EP MEDSYSTEMS ELECTROPHYSIOLOGY CATHETER
Cardiovascular
95d
Cleared
May 13, 1996
PROCATH LOCKING PEEL-AWAY INTRODUCER/PEEL-AWAY INTRODUCER SET
Cardiovascular
24d