Clearance Summary
CORE 500 Digital Stethoscope received FDA 510(k) clearance under submission number K230111, sponsored by Eko Devices, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2023-05-26.
- Submission: K230111
- Applicant / Sponsor: Eko Devices, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1875
- Decision date: 2023-05-26
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.