Clearance Summary
Strados Remote Electronic Stethoscope Platform (RESP) received FDA 510(k) clearance under submission number K220893, sponsored by Strados Labs, 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 2022-04-27.
- Submission: K220893
- Applicant / Sponsor: Strados Labs, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2800
- Decision date: 2022-04-27
Classification & Regulation
This clearance is catalogued under FDA product code DSH and 21 CFR 870.2800, within the Cardiovascular review panel as a Class II device.