meddevicedb.com FDA Device Reference

Infrared Thermometer

K202440 Class II Traditional
Decision Date
2021-06-17
Sponsor / Applicant
Shenzhen Sonida Digital Technology Co., Ltd.

Technical Specification

510(k) Submission ID K202440
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 2021-06-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Infrared Thermometer received FDA 510(k) clearance under submission number K202440, sponsored by Shenzhen Sonida Digital 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 2021-06-17.

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.