# Electro-Catheter Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 35 (1976–1995): 35 510(k) clearances
- Product codes: LDF (7), DRF (5), DXG (4), DTR (3), DQO (2), DQX (2), DYG (2), KFM (1), KYG (1), DQR (1), KNT (1), DYB (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Arrow Intl., Inc.: 2 (https://510kreport.com/company/arrow-intl)
- Zcv,Inc.: 1 (https://510kreport.com/company/zcv)
- Cardiacassist, Inc.: 1 (https://510kreport.com/company/cardiacassist)
- Heartport, Inc.: 1 (https://510kreport.com/company/heartport)

## Its most-cited devices
- K810360: Baim TM Coronary Sinus Flow Thermal (1981), cited by 1
- K832850: Elecath Pacewedge Dual Press. Bipolar (1983), cited by 1
- K844003: Elecath Ventricular Pacing Wedge Pressure Cath (1984), cited by 1
- K854511: Elecath Percutaneous Left Atrial Cannulation Set (1986), cited by 1
- K933450: Closed Tip Multi-Electrode Catheter, Modification (1995), cited by 1

## Recent decisions
- K934785: Multipace (Jul 27, 1995)
- K933450: Closed Tip Multi-Electrode Catheter, Modification (Apr 19, 1995)
- K943257: Tip Deflector (Genesis) (Apr 19, 1995)
- K933451: Open Tip Multi-Electrode Catheter, Modification (Apr 19, 1995)
- K934787: Silicore Semi-Floater (Feb 24, 1995)
- K874154: Elecath (R) Transesophageal Pacing Catheter (Apr 29, 1988)
- K854511: Elecath Percutaneous Left Atrial Cannulation Set (Feb 10, 1986)
- K854975: Elecath Pulsatile Perfusion Pump (Jan 15, 1986)

Source page: https://510kreport.com/company/electro-catheter