HeartSciences HSCS
HeartSciences gets FDA clearance for MyoVista device
Additional proxy materials
- Form
- DEFA14A
- Filed
- Importance
- Routine
- Accession
- 0001213900-26-107250
- FDA granted 510(k) clearance (K260005) for MyoVista wavECG device
- Clearance covers ECG signal acquisition and interpretation for adult and pediatric patients
- Device does not include AI-ECG algorithm
- Company plans to evaluate device and IP options
Written from the DEFA14A on EDGAR. Check the filing before you rely on it.
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