Clearance Summary
AccurSound Electronic Stethoscope AS-101 received FDA 510(k) clearance under submission number K221805, sponsored by Heroic Faith International , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2023-03-23.
- Submission: K221805
- Applicant / Sponsor: Heroic Faith International , Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1875
- Decision date: 2023-03-23
Classification & Regulation
This clearance is catalogued under FDA product code DQD and 21 CFR 870.1875, within the Cardiovascular review panel as a Class II device.