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Non-contact Infrared Thermometer (Models WL-301, WL-501, WL-601, WL-701)

K210171 Class II Traditional
Decision Date
2022-03-18
Sponsor / Applicant
Sichuan Youkede Medical Equipment Co.,Ltd

Technical Specification

510(k) Submission ID K210171
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 2022-03-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Non-contact Infrared Thermometer (Models WL-301, WL-501, WL-601, WL-701) received FDA 510(k) clearance under submission number K210171, sponsored by Sichuan Youkede Medical Equipment 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 2022-03-18.

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.