Clearance Summary
MICROTHERM MT-501 & MT-502 received FDA 510(k) clearance under submission number K854007, sponsored by Medequi, Division of King Yip Co., 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 1985-11-08.
- Submission: K854007
- Applicant / Sponsor: Medequi, Division of King Yip Co., Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.2910
- Decision date: 1985-11-08
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.