LiDCO Ltd Li10800
LiDCO Ltd Li10800 is a Class II device made by Lidco Limited, cleared under FDA 510(k) K122247 on 20 Mar 2013 and listed in FDA GUDID since 29 Nov 2017 (UDI-DI 05060110521586), 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 | Number05060110521586 | Date29 Nov 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK122247 | Date20 Mar 2013 | StatusActive |
Official records
- AccessGUDID record 05060110521586
- FDA 510(k) database K122247
Across registries
- FDA 510(k) K122247 decided 20 Mar 2013 Active
- FDA GUDID UDI-DI 05060110521586 listed 29 Nov 2017 Listed
Timeline
- Cleared FDA 510(k) K122247
- Listed FDA GUDID 05060110521586
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- Withdrawn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
- Li10800
- Primary DI / UDI-DI
- 05060110521586
- 510(k) Number
- FDA product code
- GWQ
- GMDN term
- General-purpose multi-parameter bedside monitor
- Device class
- Class II
- Regulation number
- 882.1400
- GUDID distribution status
- In Commercial Distribution