- All Devices
- Cardiology
- SENSICARDIAC MOBI DIAGNOSTIC HEART MURMUR APPLICATION
Cardiology
SENSICARDIAC MOBI DIAGNOSTIC HEART MURMUR APPLICATION
DIACOUSTIC MEDICAL DEVICES (PTY) LTD.
FDA-cleared AI medical device
FDA Submission Metadata
- Submission number
- K131044
- Decision date
- September 2013
- FDA panel
- Cardiovascular
- Product code
- DQD
This entry is sourced from the FDA AI/ML-Enabled Medical Devices list. No editorial review yet — the catalogue may add a deeper review of this device in future.
This entry is on our editorial review queue. Full evaluation — performance metrics, clinical evidence, safety record — lands as our review pipeline graduates each device. The information above is what's been verified to date.