meddevicedb.com FDA Device Reference

MICRO THERM MT-500 & MT-600

K854035 Class II Traditional
Decision Date
1985-11-12
Sponsor / Applicant
Medequi, Division of King Yip Co., Inc.

Technical Specification

510(k) Submission ID K854035
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 1985-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICRO THERM MT-500 & MT-600 received FDA 510(k) clearance under submission number K854035, 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 1985-11-12.

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.