Fluido® AirGuard System

FDA 510(k) K251733 · The Surgical Company International BV (As Tsc Life)

Substantially Equivalent

510(k) numberK251733

Submission

Device name
Fluido® AirGuard System
Applicant
The Surgical Company International BV (As Tsc Life)
Amsterdam, NL
Received
June 6, 2025
Decision date
September 4, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LGZ – Warmer, Thermal, Infusion Fluid
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5725
Specialty
General Hospital

Other 510(k)s with product code LGZ

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K260988°M Warmer System with °M StationLGZ · Special Mequ A/S04/24/2026SE
K252636Fluido Compact SystemLGZ · Traditional The Surgical Company International B.V.11/18/2025SE
K232107°M Warmer SystemLGZ · Traditional Mequ A/S05/31/2024SE
K211618Fluido Compact Blood and Fluid Warming SystemLGZ · Traditional The Surgical Company International B.V.06/05/2023SE
K211800Warrior Blood and Fluid Warmer, Warrior EXTREME Blood and Fluid Warmer, Warrior Lite…LGZ · Traditional Quality IN Flow , Ltd.12/08/2022SE
K202461ThermaCor 1200 Disposable Sets for the ThermaCor 1200 Rapid Thermal Infusion SystemLGZ · Traditional Smisson-Cartledge Biomedical, LLC08/12/2022SE
K213191S-LineLGZ · Traditional Barkey GmbH & Co. KG05/24/2022SE
K192325Quantum Blood and Fluid Warming SystemLGZ · Special Life Warmer, Inc.10/18/2019SE
K180842MAC Medical D-Series Blanket and Solution Warming CabinetsLGZ · Traditional Mac Medical, Inc.03/05/2019SE
K181775Quantum Blood and IV Fluid Infusion WarmerLGZ · Traditional Life Warmer, Inc.01/28/2019SE

Questions and answers

When was Fluido® AirGuard System cleared by the FDA?

Fluido® AirGuard System (K251733) received a 510(k) decision of Substantially Equivalent on September 4, 2025, 90 days after the submission was received.

What is the product code of K251733?

The FDA product code is LGZ – Warmer, Thermal, Infusion Fluid, a Class II (moderate risk) device regulated under 21 CFR 880.5725.