Fever therometer MP-TM21-US
Fever therometer MP-TM21-US is a Class II device made by Better Basics, Inc., cleared under FDA 510(k) K103407 on 13 May 2011 and listed in FDA GUDID since 18 Nov 2016 (UDI-DI 00817746020243), 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 | Number00817746020243 | Date18 Nov 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK103407 | Date13 May 2011 | StatusActive |
Official records
- AccessGUDID record 00817746020243
- FDA 510(k) database K103407
Across registries
- FDA 510(k) K103407 decided 13 May 2011 Active
- FDA GUDID UDI-DI 00817746020243 listed 18 Nov 2016 Listed
Timeline
- Cleared FDA 510(k) K103407
- Listed FDA GUDID 00817746020243
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Fever therometer
- Generic name
- Infrared patient thermometer, skin
- Model / reference
- MP-TM21-US
- Primary DI / UDI-DI
- 00817746020243
- 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
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