# Padpro, LLC

- Location (FDA's records): Deer Field, IL
- FDA decisions: 5 (2001–2002): 5 510(k) clearances
- Product codes: MKJ (5)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 6 (1 its own)
- Recalls linked to its devices: 9 (6 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Katecho, Inc.: 2 (https://510kreport.com/company/katecho)
- Medical Devices, Inc.: 1 (https://510kreport.com/company/medical-devices)

## Firms that cite its devices most
- Heart Sync, Inc.: 2 (https://510kreport.com/company/heart-sync)
- Cardio Medical Products, Inc.: 2 (https://510kreport.com/company/cardio-medical-products)
- Leonhard Lang GmbH: 1 (https://510kreport.com/company/leonhard-lang)

## Its most-cited devices
- K020203: Padpro Model #2516 (2002), cited by 3
- K014209: Padpro  Model 2001, 2001-S, 2001-C, 2001-Eps (2002), cited by 2
- K020288: Padpro, Model 2603 (2002), cited by 1

## Recent decisions
- K020743: Padpro, Model 2502 (May 28, 2002)
- K020203: Padpro Model #2516 (May 8, 2002)
- K020288: Padpro, Model 2603 (Feb 27, 2002)
- K014209: Padpro  Model 2001, 2001-S, 2001-C, 2001-Eps (Jan 18, 2002)
- K003548: Padpro System Defibrillator Electrode Adapters (Sep 4, 2001)

Source page: https://510kreport.com/company/padpro