Conair ITH90
by Conair LLC.
Conair ITH90 is a Class II device made by Conair LLC., cleared under FDA 510(k) K140681 on 21 Aug 2014 and listed in FDA GUDID since 17 Jul 2023 (UDI-DI 00074108454584), active as of 23 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 | Number00074108454584 | Date17 Jul 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK140681 | Date21 Aug 2014 | StatusActive |
Official records
- AccessGUDID record 00074108454584
- FDA 510(k) database K140681
Across registries
- FDA 510(k) K140681 decided 21 Aug 2014 Active
- FDA GUDID UDI-DI 00074108454584 listed 17 Jul 2023 Listed
Timeline
- Cleared FDA 510(k) K140681
- Listed FDA GUDID 00074108454584
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Conair
- Generic name
- Infrared patient thermometer, ear/skin
- Model / reference
- ITH90
- Primary DI / UDI-DI
- 00074108454584
- 510(k) Number
- FDA product code
- FLL
- GMDN term
- Infrared patient thermometer, ear/skin
- Device class
- Class II
- Regulation number
- 880.2910
- GUDID distribution status
- In Commercial Distribution
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