LiDCO Ltd Li10705
LiDCO Ltd Li10705 is a Class II device made by Lidco Limited, cleared under FDA 510(k) K131048 on 28 Aug 2013 and listed in FDA GUDID since 13 Sep 2016 (UDI-DI 05060110521081), 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 | Number05060110521081 | Date13 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK131048 | Date28 Aug 2013 | StatusActive |
Official records
- AccessGUDID record 05060110521081
- FDA 510(k) database K131048
Across registries
- FDA 510(k) K131048 decided 28 Aug 2013 Active
- FDA GUDID UDI-DI 05060110521081 listed 13 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K131048
- Listed FDA GUDID 05060110521081
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- LiDCO Ltd
- Generic name
- General-purpose multi-parameter bedside monitor
- Model / Ref / Catalog
- Li10705
- Primary DI / UDI-DI
- 05060110521081
- 510(k) Number
- FDA product code
- DXG
- GMDN term
- General-purpose multi-parameter bedside monitor
- Device class
- Class II
- Regulation number
- 870.1435
- GUDID distribution status
- In Commercial Distribution