510(k) DEN250044
DEN250044 is an FDA 510(k) premarket notification submitted by Powerful Medical, Inc. for the device "STEMI AI ECG Model". The FDA issued a decision of De Novo Granted on Sep 3, 2026.
Clearance Details
- Decision
- DENG (De Novo Granted)
- Decision Date
- Sep 3, 2026
- Date Received
- Sep 22, 2025
- Clearance Type
- Direct
- Expedited Review
- No
- Third Party Review
- No