# Cardiac Control Systems, Inc.

- Location (FDA's records): Palm Coast, FL
- FDA decisions: 28 (1983–1997): 26 510(k) clearances and 2 original PMA approvals
- Product codes: DXY (15), DTB (9), DTG (1), DTD (1), LDF (1), LWP (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (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 whose devices it cites most
- Cordis Corp.: 1 (https://510kreport.com/company/cordis)

## Recent decisions
- K971775: Interim AV Shaped Temporary Pacing Catheter Model Int-AV610 (Dec 29, 1997)
- K946188: CCDS Maestro (R) II Series 200 Cadiac Pacemaker (May 15, 1995)
- K950210: CCS Maestro (R) II Series 200 Models 235 and 227 Cardiac Pacemaker (May 3, 1995)
- K923868: CCS Maestro II Series 200 Cardiac Pacemaker (May 14, 1993)
- K905824: Maestro (R) Series 100/200 Cardiac S/Chamb Pacemake (May 16, 1991)
- K904941: Maestro Series 100/200 Cardiac Single Chamber Pace (Jan 3, 1991)
- P890039: Mastro Savvi Series 300 VDD Pacing System (Sep 25, 1990)
- K895110: Maestro Pacemaker Test Magnet (Sep 26, 1989)

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