# Katecho, Inc.

- Location (FDA's records): Des Moines, IA
- FDA decisions: 26 (1984–2001): 26 510(k) clearances
- Product codes: MKJ (7), DRO (4), GXY (4), LDD (4), GZJ (3), DRX (2), ELE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 13 (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 that cite its devices most
- Cardio Medical Products, Inc.: 2 (https://510kreport.com/company/cardio-medical-products)
- Survivalink Corp.: 2 (https://510kreport.com/company/survivalink)
- Padpro, LLC: 2 (https://510kreport.com/company/padpro)
- Technomed Europe: 1 (https://510kreport.com/company/technomed-europe)
- Heartsine Technologies, Inc.: 1 (https://510kreport.com/company/heartsine-technologies)
- Heart Sync, Inc.: 1 (https://510kreport.com/company/heart-sync)
- Transfer Technology: 1 (https://510kreport.com/company/transfer-technology)
- Defibtech, LLC: 1 (https://510kreport.com/company/defibtech)

## Its most-cited devices
- K981737: K-Defib/Pace Adult Electrode Model Number KDP-60 (1998), cited by 6
- K000870: KM-10 Tens Electrode (2000), cited by 2
- K002806: K-Defib/Pace, Model KDP-60A (2000), cited by 2
- K914955: K-Defib/Pace Electrode (1992), cited by 1
- K900997: K-Sterile Tens Electrodes (1990), cited by 1
- K954504: K-Defib/Pace Pediatric Electrode (1995), cited by 1

## Recent decisions
- K012404: K-Defib/Pace Adult Electrode, Model KDP-85 (Oct 12, 2001)
- K010543: KM-30 Tens Electrode (May 23, 2001)
- K003228: K-Defib/Pace Multifuction Pediatric Electrode, Model KDP-70A (Dec 14, 2000)
- K002806: K-Defib/Pace, Model KDP-60A (Nov 21, 2000)
- K000870: KM-10 Tens Electrode (Nov 7, 2000)
- K993745: K-Defib/Pace Adult Electrode, Model KDP-80 (Feb 3, 2000)
- K991007: K-Defib/Pace Radiolucent Adult Electrode, Model KRT-60 (Aug 23, 1999)
- K981737: K-Defib/Pace Adult Electrode Model Number KDP-60 (Dec 9, 1998)

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