Ep Technologies, Inc. is one of 23726 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ep Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: REAL-TIME POSITION MANAGEMENT (RPM) SYSTEM, ASTRONOMER PLUS SYSTEM, POLARIS X CATHETERS, MODEL 7000D,7001D,7003D,7004D,7005D,7006D
15
Total
15
Cleared
0
Denied
Ep Technologies, Inc. has 15 FDA 510(k) cleared cardiovascular devices. Based in Mountain View, US.
Historical record: 15 cleared submissions from 1988 to 2005.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ep Technologies, Inc.
15 devices
Cleared
Feb 03, 2005
REAL-TIME POSITION MANAGEMENT (RPM) SYSTEM
Cardiovascular
71d
Cleared
Apr 09, 2002
ASTRONOMER PLUS SYSTEM
Cardiovascular
182d
Cleared
Dec 07, 2000
POLARIS X CATHETERS, MODEL 7000D,7001D,7003D,7004D,7005D,7006D
Cardiovascular
30d
Cleared
Aug 02, 1994
DIAGNOSTIC I CATHETER
Cardiovascular
207d
Cleared
Jul 27, 1994
DIAGNOSTIC II CATHETER
Cardiovascular
201d
Cleared
Dec 16, 1993
TRACFINDER II
Cardiovascular
489d
Cleared
Dec 16, 1993
STEEROCATH II
Cardiovascular
489d
Cleared
Oct 25, 1991
TORQUE TUBE STEEROCATH(TM)
Cardiovascular
88d
Cleared
Oct 12, 1990
FRANZ(TM) STEERABLE COMBINATION CATHETER
Cardiovascular
51d
Cleared
May 07, 1990
STEEROCATH(TM)
Cardiovascular
80d
Cleared
Mar 14, 1990
QUATTRO CATHETER
Cardiovascular
43d
Cleared
Mar 13, 1990
CONSTANT CURRENT STIMULATOR MODEL 022101
Cardiovascular
35d