Mobi 700026
Mobi 700026 is a Class II device made by Mobi Technologies, Inc., cleared under FDA 510(k) K172795 on 14 Mar 2018 and listed in FDA GUDID since 31 Jul 2022 (UDI-DI 00891040000262), 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 | Number00891040000262 | Date31 Jul 2022 | StatusListed |
| United States | FDA 510(k) | NumberK172795 | Date14 Mar 2018 | StatusActive |
Official records
- AccessGUDID record 00891040000262
- FDA 510(k) database K172795
Across registries
- FDA 510(k) K172795 decided 14 Mar 2018 Active
- FDA GUDID UDI-DI 00891040000262 listed 31 Jul 2022 Listed
Timeline
- Cleared FDA 510(k) K172795
- Listed FDA GUDID 00891040000262
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Mobi
- Generic name
- Infrared patient thermometer, ear/skin
- Model / reference
- 700026
- Primary DI / UDI-DI
- 00891040000262
- 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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