Clearance Summary
Tyto Stethoscope received FDA 510(k) clearance under submission number K160401, sponsored by Tyto Care , 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 2016-10-19.
- Submission: K160401
- Applicant / Sponsor: Tyto Care , Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1875
- Decision date: 2016-10-19
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.