Medical Device Manufacturer · US , Sunnyvale , CA

Cardiac Pathways Corp. - FDA 510(k) Cleared Devices

5 submissions · 4 cleared · Since 1997

Recent clearances: CARDIAC PATHWAYS REFERENCE CATHETER AND REFERENCE CATHETER WITH TRACKING, CARDIAC PATHWAYS RADII CATHETER AND RADII CATH, MERCATOR ATRIAL HIGH DENSITY ARRAY CATHETER, MERCATOR ATRIAL HIGH DENSITY ARRAY CATHETER MODELS, 7005, 7006, 7007, MERCATOR ATRIAL HIGH DENSITY ARRAY DEPLOYMENT KIT,

View 5 510(k) 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.

Cardiac Pathways Corp. is one of 21905 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cardiac Pathways Corp.

5 devices

1-5 of 5

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