Cleared Traditional

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

K232128 · Shenzhen AOJ Medical Technology Co., Ltd. · General Hospital
Oct 2023
Decision
89d
Days
Class 2
Risk

About This 510(k) Submission

K232128 is an FDA 510(k) clearance for the Infrared Thermometer (AOJ-20A); Infrared Thermometer (AOJ-20Y), a Continuous Measurement Thermometer (Class II — Special Controls, product code FLL), submitted by Shenzhen AOJ Medical Technology Co., Ltd. (Shenzhen, CN). The FDA issued a Cleared decision on October 14, 2023, 89 days after receiving the submission on July 17, 2023. This device falls under the General Hospital review panel. Regulated under 21 CFR 880.2910.

Submission Details

510(k) Number K232128 FDA.gov
FDA Decision Cleared SESE
Date Received July 17, 2023
Decision Date October 14, 2023
Days to Decision 89 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF

Device Classification

Product Code FLL — Continuous Measurement Thermometer
Device Class Class II — Special Controls
CFR Regulation 21 CFR 880.2910
Definition A Continuous Measurement Thermometer Is A Clinical Electronic Thermometer Indicated To Measure The Body Or Skin Temperature Of A Person Continuously Or In Specified Intervals. Under This Regulation, This Product Code Represents Non-exempt Devices. For More Information, See 90 Fr 25889, Available At Https://www.govinfo.gov/content/pkg/fr-2025-06-18/pdf/2025-11207.pdf.

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