Clearance Summary
ibiomedi Electronic Stethoscope ES-2020 received FDA 510(k) clearance under submission number K220466, sponsored by Sound Land Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2022-11-03.
- Submission: K220466
- Applicant / Sponsor: Sound Land Corp.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1875
- Decision date: 2022-11-03
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.