Quantum Blood and IV Fluid Infusion Warmer

FDA 510(k) K181775 · Life Warmer, Inc.

Substantially Equivalent

510(k) numberK181775

Submission

Device name
Quantum Blood and IV Fluid Infusion Warmer
Applicant
Life Warmer, Inc.
Plano, TX, US
Received
July 3, 2018
Decision date
January 28, 2019
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

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Questions and answers

When was Quantum Blood and IV Fluid Infusion Warmer cleared by the FDA?

Quantum Blood and IV Fluid Infusion Warmer (K181775) received a 510(k) decision of Substantially Equivalent on January 28, 2019, 209 days after the submission was received.

What is the product code of K181775?

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