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LiDCO Ltd Li11057

by Lidco Limited

LiDCO Ltd Li11057 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 30 Nov 2016 (UDI-DI 05060110522194), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US), not in commercial distribution.

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K122247

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05060110522194 UDI-DI Date30 Nov 2016ListedStatusListed GUDID: not in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK122247 Date20 Mar 2013DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K122247 decided 20 Mar 2013 Active
  • FDA GUDID UDI-DI 05060110522194 listed 30 Nov 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K122247
  2. Listed FDA GUDID 05060110522194

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
LiDCO Ltd
Generic name
General-purpose multi-parameter bedside monitor
Model / Ref / Catalog
Li11057
Primary DI / UDI-DI
05060110522194
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
Not in Commercial Distribution

Other devices from Lidco Limited

  • LiDCO Li11083

    Class II
  • LiDCO Ltd Li10707

    Class II
  • LiDCO Ltd Li10395

    Class II
  • LiDCO Ltd CM 50-001-01

    Class II

See all devices from Lidco Limited →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)