Clearance Summary
ANSWATCH WRIST MONITOR MODEL TS-0411 received FDA 510(k) clearance under submission number K123130, sponsored by Taiwan Scientific Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2013-09-17.
- Submission: K123130
- Applicant / Sponsor: Taiwan Scientific Corporation
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1130
- Decision date: 2013-09-17
Classification & Regulation
This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.