# Access Cardiosystems, Inc.

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

## Firms whose devices it cites most
- Agilent Technologies, Inc.: 1 (https://510kreport.com/company/agilent-technologies)
- Physio-Control Corp.: 1 (https://510kreport.com/company/physio-control)
- ZOLL Medical Corporation: 1 (https://510kreport.com/company/zoll-medical)

## Recent decisions
- K020984: Accessaed, Semi-Automatic External Defibrillators (Aug 14, 2002)
- K011461: Access Cardiosystems Manual Defibrillator (May 28, 2002)

Source page: https://510kreport.com/company/access-cardiosystems