meddevicedb.com FDA Device Reference

Infrared Thermometer (AOJ-20A); Infrared Thermometer (AOJ-20Y)

K232128 Class II Traditional
Decision Date
2023-10-14
Sponsor / Applicant
Shenzhen AOJ Medical Technology Co., Ltd.

Technical Specification

510(k) Submission ID K232128
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 2023-10-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Infrared Thermometer (AOJ-20A); Infrared Thermometer (AOJ-20Y) received FDA 510(k) clearance under submission number K232128, sponsored by Shenzhen AOJ Medical 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 2023-10-14.

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.