# Diacoustic Medical Devices (Pty), Ltd.

- Location (FDA's records): Crofton, MD
- FDA decisions: 2 (2011–2013): 2 510(k) clearances
- Product codes: DQD (2)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 4 (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
- Diacoustic Medical (Pty): 1 (https://510kreport.com/company/diacoustic-medical)
- Zargis Medical Corp.: 1 (https://510kreport.com/company/zargis-medical)
- Meditron AS: 1 (https://510kreport.com/company/meditron)

## Firms that cite its devices most
- Eko Devices, Inc.: 1 (https://510kreport.com/company/eko-devices)
- Csd Labs GmbH: 1 (https://510kreport.com/company/csd-labs)
- Rijuven Corp: 1 (https://510kreport.com/company/rijuven)
- Diacoustic Medical (Pty): 1 (https://510kreport.com/company/diacoustic-medical)

## Its most-cited devices
- K131044: Sensicardiac Mobi Diagnostic Heart Murmur Application (2013), cited by 2
- K110704: SENSI (2011), cited by 2

## Recent decisions
- K131044: Sensicardiac Mobi Diagnostic Heart Murmur Application (Sep 4, 2013)
- K110704: SENSI (Jun 24, 2011)

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