meddevicedb.com FDA Device Reference

GERATHERM MERCUIRY FREE CLINICAL THERMOMETER

K960224 Class II Traditional
Decision Date
1996-03-25
Sponsor / Applicant
Rg Ent., Inc.

Technical Specification

510(k) Submission ID K960224
Product Code FLK
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2920
Decision Date 1996-03-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GERATHERM MERCUIRY FREE CLINICAL THERMOMETER received FDA 510(k) clearance under submission number K960224, sponsored by Rg Ent., 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 1996-03-25.

Classification & Regulation

This clearance is catalogued under FDA product code FLK and 21 CFR 880.2920, within the General Hospital review panel as a Class II device.