Clearance Summary
HeRO Symphony, HeRO ES, HeRO solo/duet received FDA 510(k) clearance under submission number K180242, sponsored by Medical Predictive Science Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2018-02-28.
- Submission: K180242
- Applicant / Sponsor: Medical Predictive Science Corporation
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2340
- Decision date: 2018-02-28
Classification & Regulation
This clearance is catalogued under FDA product code DPS and 21 CFR 870.2340, within the Cardiovascular review panel as a Class II device.