# Cardio Medical Products, Inc.

- Location (FDA's records): Rockaway, NJ
- FDA decisions: 3 (2011–2011): 3 510(k) clearances
- Product codes: LDD (3)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Heart Sync, Inc.: 2 (https://510kreport.com/company/heart-sync)
- Padpro, LLC: 2 (https://510kreport.com/company/padpro)
- Katecho, Inc.: 2 (https://510kreport.com/company/katecho)

## Recent decisions
- K103651: Cardiomed (Oct 4, 2011)
- K103334: Cardio Med (Jan 18, 2011)
- K103159: Cardio Med Model A102, H104, O101, P103, and Z100 (Jan 11, 2011)

Source page: https://510kreport.com/company/cardio-medical-products