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 |
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.
| 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 |
| 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. |