# Medical Devices/Padpro, Inc.

- Location (FDA's records): Deer Field, IL
- FDA decisions: 1 (2006–2006): 1 510(k) clearance
- Product codes: DRG (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
- Physio-Control Corp.: 1 (https://510kreport.com/company/physio-control)

## Recent decisions
- K061606: Defibrillator Cable Tester, Model DT2200 (Jun 21, 2006)

Source page: https://510kreport.com/company/medical-devices-padpro