# Cardiac Pathways Corp.

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 5 (1997–2000): 5 510(k) clearances
- Product codes: DRF (3), MTD (2)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Ep Technologies, Inc.: 2 (https://510kreport.com/company/ep-technologies)

## Its most-cited devices
- K992912: Cardiac Pathways Reference Catheter and Reference Catheter with Tracking, Cardiac Pathways Radii Catheter and Radii Cath (2000), cited by 2
- K982540: Mercator Atrial High Density Array Catheter Models, 7005, 7006, 7007, Mercator Atrial High Density Array Deployment Kit, (1999), cited by 1

## Recent decisions
- K992912: Cardiac Pathways Reference Catheter and Reference Catheter with Tracking, Cardiac Pathways Radii Catheter and Radii Cath (Mar 8, 2000)
- K990795: Mercator Atrial High Density Array Catheter; Cardiac Pathways Egm Adapter Cables (Jun 8, 1999)
- K982540: Mercator Atrial High Density Array Catheter Models, 7005, 7006, 7007, Mercator Atrial High Density Array Deployment Kit, (Jan 27, 1999)
- K983653: Radii Diagnostic Electrophysiology Catheter, Model # 30411 B, C and D (Dec 22, 1998)
- K965066: Arrhythmia Mapping System (8100/8300) (Aug 11, 1997)

Source page: https://510kreport.com/company/cardiac-pathways