Clearance Summary
DIGITAL THERMOMETER, MODELS MT-XX8 AND MT-XX9 received FDA 510(k) clearance under submission number K041516, sponsored by Vega Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2004-09-08.
- Submission: K041516
- Applicant / Sponsor: Vega Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.2910
- Decision date: 2004-09-08
Classification & Regulation
This clearance is catalogued under FDA product code FLL and 21 CFR 880.2910, within the General Hospital review panel as a Class II device.