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Digital thermometer, Model DT101, DT102

K213746 Class II Traditional
Decision Date
2022-04-05
Sponsor / Applicant
Guangzhou Berrcom Medical Device Co., Ltd.

Technical Specification

510(k) Submission ID K213746
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 2022-04-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Digital thermometer, Model DT101, DT102 received FDA 510(k) clearance under submission number K213746, sponsored by Guangzhou Berrcom Medical Device 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 2022-04-05.

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.