Clearance Summary
DIGITAL CLINICAL THERMOMETER ST-813A, ST-814A, ST-823 AND ST-823A received FDA 510(k) clearance under submission number K962520, sponsored by Mesure Technology. 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 1996-09-12.
- Submission: K962520
- Applicant / Sponsor: Mesure Technology
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.2910
- Decision date: 1996-09-12
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.