meddevicedb.com FDA Device Reference

RAPID DIGITAL THERMOMETER, MODEL RDT -18 SERIES

K062010 Class II Traditional
Decision Date
2006-10-27
Sponsor / Applicant
Global Treasure Industries , Ltd.

Technical Specification

510(k) Submission ID K062010
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 2006-10-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RAPID DIGITAL THERMOMETER, MODEL RDT -18 SERIES received FDA 510(k) clearance under submission number K062010, sponsored by Global Treasure Industries , Ltd.. 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 2006-10-27.

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.