meddevicedb.com FDA Device Reference

DT100 Digital Thermometer

K203731 Class II Traditional
Decision Date
2021-09-26
Sponsor / Applicant
Smart Technology Co., Ltd.

Technical Specification

510(k) Submission ID K203731
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 2021-09-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DT100 Digital Thermometer received FDA 510(k) clearance under submission number K203731, sponsored by Smart Technology Co., 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 2021-09-26.

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.