# Cardiac Assist Devices, Inc.

- Location (FDA's records): Cleveland, OH
- FDA decisions: 3 (1997–2002): 3 510(k) clearances
- Product codes: DRF (2), DTG (1)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Cordis Webster, Inc.: 2 (https://510kreport.com/company/cordis-webster)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- Ep Technologies, Inc.: 1 (https://510kreport.com/company/ep-technologies)

## Its most-cited devices
- K955847: Gyro Tip EP Catheter (1997), cited by 1

## Recent decisions
- K012520: Gyro-Tip Lariat Deflectable Loop Mapping Catheter, Model GTL-20E (Mar 27, 2002)
- K960849: Magno Alarm (Mar 26, 1997)
- K955847: Gyro Tip EP Catheter (Jan 29, 1997)

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