# Caditec AG

- Location (FDA's records): Mundelein, IL
- FDA decisions: 1 (1999–1999): 1 510(k) clearance
- Product codes: DQD (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 6 (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
- Delphi Consulting Group: 1 (https://510kreport.com/company/delphi-consulting-group)
- Schiller America, Inc.: 1 (https://510kreport.com/company/schiller-america)

## Firms that cite its devices most
- Meditron AS: 1 (https://510kreport.com/company/meditron)
- Pulsonic Ag, Medical Technology: 1 (https://510kreport.com/company/pulsonic-ag-medical-technology)
- Hd Medical Services (India) Pvt.Ltd: 1 (https://510kreport.com/company/hd-medical-services-india-pvt)
- Techtrade, LLC: 1 (https://510kreport.com/company/techtrade)
- Zargis Medical Corp.: 1 (https://510kreport.com/company/zargis-medical)
- Colin Corp.: 1 (https://510kreport.com/company/colin)

## Its most-cited devices
- K990809: Cadiscope Electronic Stethoscope (1999), cited by 6

## Recent decisions
- K990809: Cadiscope Electronic Stethoscope (Jun 9, 1999)

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