Medtronic Cardiorhythm - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Medtronic Cardiorhythm has 5 FDA 510(k) cleared medical devices. Based in San Jose, US.
Historical record: 5 cleared submissions from 1994 to 1998. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medtronic Cardiorhythm Filter by specialty or product code using the sidebar.
5 devices
Cleared
Aug 05, 1998
STABLEMAPR STEERABLE INTRACARDIAC CATHETERS
Cardiovascular
89d
Cleared
Jan 23, 1997
PERFORMR SERIES EP DIAGNOSTIC CATHETERS
Cardiovascular
90d
Cleared
Apr 15, 1996
PLATINUM SERIES EP DIAGNOSTIC CATHETERS
Cardiovascular
280d
Cleared
May 10, 1995
MARINR SERIES EP DIAGNOSTI CATHETERS
Cardiovascular
71d
Cleared
Jun 06, 1994
MARINR SERIES EP DIAGNOSTIC CATHETERS
Cardiovascular
420d