Cardiac Pathways Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardiac Pathways Corp. - FDA 510(k) Cleared Devices
5
Total
4
Cleared
0
Denied
Cardiac Pathways Corp. has 4 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 4 cleared submissions from 1997 to 2000. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardiac Pathways Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardiac Pathways Corp.
5 devices
Cleared
Mar 08, 2000
CARDIAC PATHWAYS REFERENCE CATHETER AND REFERENCE CATHETER WITH TRACKING,...
Cardiovascular
191d
Cleared
Jun 08, 1999
MERCATOR ATRIAL HIGH DENSITY ARRAY CATHETER
Cardiovascular
90d
Cleared
Jan 27, 1999
MERCATOR ATRIAL HIGH DENSITY ARRAY CATHETER MODELS, 7005, 7006, 7007,...
Cardiovascular
190d
Cleared
Dec 22, 1998
RADII DIAGNOSTIC ELECTROPHYSIOLOGY CATHETER, MODEL # 30411 B, C AND D
Cardiovascular
64d
Cleared
Aug 11, 1997
ARRHYTHMIA MAPPING SYSTEM (8100/8300)
Cardiovascular
236d