Clearance Summary
V-TRUST HANDHELD PULSE OXIMETER MODEL: TD-8201 received FDA 510(k) clearance under submission number K101012, sponsored by Taidoc Technology 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 2010-12-15.
- Submission: K101012
- Applicant / Sponsor: Taidoc Technology Corporation
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2700
- Decision date: 2010-12-15
Classification & Regulation
This clearance is catalogued under FDA product code DQA and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.