# Lidco, Ltd.

- Location (FDA's records): London, GB
- FDA decisions: 7 (1999–2017): 7 510(k) clearances
- Product codes: DXG (7)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 7 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- American Edwards Laboratories: 1 (https://510kreport.com/company/american-edwards-laboratories)
- Edwards Laboratories: 1 (https://510kreport.com/company/edwards-laboratories)

## Firms that cite its devices most
- Transonic Systems, Inc.: 4 (https://510kreport.com/company/transonic-systems)
- Retia Medical, LLC: 1 (https://510kreport.com/company/retia-medical)
- Icu Medical, Inc.: 1 (https://510kreport.com/company/icu-medical)
- Masimo Corporation: 1 (https://510kreport.com/company/masimo)

## Its most-cited devices
- K023960: Lidcoplus Hemodynamic Monitor System, Model HM 70 (2003), cited by 4
- K122247: Lidcorapid V2 Monitor (2013), cited by 1
- K163334: LiDCOunity v2 Hemodynamic Monitor (2017), cited by 1
- K010049: Pulseco Hemodynamic Monitor CM71 (2001), cited by 1

## Recent decisions
- K163334: LiDCOunity v2 Hemodynamic Monitor (Jun 5, 2017)
- K152935: LiDCOunity Monitor (Mar 17, 2016)
- K131048: Lidco Cnap Module (Aug 28, 2013)
- K122247: Lidcorapid V2 Monitor (Mar 20, 2013)
- K023960: Lidcoplus Hemodynamic Monitor System, Model HM 70 (Jan 9, 2003)
- K010049: Pulseco Hemodynamic Monitor CM71 (Jun 14, 2001)
- K962918: Lidco System (Jan 8, 1999)

Source page: https://510kreport.com/company/lidco