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INFRARED EAR THERMOMETER, MODEL DX-707

K013876 Class II Traditional
Decision Date
2002-03-04
Sponsor / Applicant
Jawon Medical Co., Ltd.

Technical Specification

510(k) Submission ID K013876
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 2002-03-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INFRARED EAR THERMOMETER, MODEL DX-707 received FDA 510(k) clearance under submission number K013876, sponsored by Jawon Medical 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 2002-03-04.

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.