Infrared Thermometer FR820
by Shenzhen Jiacom Technology Co., Ltd
Infrared Thermometer FR820 is a Class II device made by Shenzhen Jiacom Technology Co., Ltd, cleared under FDA 510(k) K172874 on 12 Jul 2018 and listed in FDA GUDID since 28 Oct 2020 (UDI-DI 06953205900870), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number06953205900870 | Date28 Oct 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK172874 | Date12 Jul 2018 | StatusActive |
Official records
- AccessGUDID record 06953205900870
- FDA 510(k) database K172874
Across registries
- FDA 510(k) K172874 decided 12 Jul 2018 Active
- FDA GUDID UDI-DI 06953205900870 listed 28 Oct 2020 Listed
Timeline
- Cleared FDA 510(k) K172874
- Listed FDA GUDID 06953205900870
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Infrared Thermometer
- Generic name
- Infrared patient thermometer, skin
- Model / reference
- FR820
- Primary DI / UDI-DI
- 06953205900870
- 510(k) Number
- FDA product code
- FLL
- GMDN term
- Infrared patient thermometer, skin
- Device class
- Class II
- Regulation number
- 880.2910
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Infrared patient thermometer, skin.