Quantum Blood and Fluid Warming System

FDA 510(k) K192325 · Life Warmer, Inc.

Substantially Equivalent

510(k) numberK192325

Submission

Device name
Quantum Blood and Fluid Warming System
Applicant
Life Warmer, Inc.
Addison, TX, US
Received
August 27, 2019
Decision date
October 18, 2019
Decision
Substantially Equivalent (SESE)
Type
Special 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

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Questions and answers

When was Quantum Blood and Fluid Warming System cleared by the FDA?

Quantum Blood and Fluid Warming System (K192325) received a 510(k) decision of Substantially Equivalent on October 18, 2019, 52 days after the submission was received.

What is the product code of K192325?

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