# K023653: Maxone IV Fluid/Blood Warmer, Model 102

- Pathway: 510(k) (Traditional)
- Applicant: Automatic Medical Technologies, Inc.
- Decided: Jan 17, 2003 after 79 days
- Product code: LGZ (Warmer, Thermal, Infusion Fluid)
- Device class: 2
- Regulation: 21 CFR 880.5725
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K002409 (2001). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K002409: Maxone, Blood, Blood Products and IV Fluid Warmer, Automatic Medical Technologies, Inc. (2001) Summary page 1.

## Indications for use
The MaxOneTMIV Fluid/Blood Warmer, Model 102, is indicated for the warming of blood products and intravenous solutions prior to administration. It is intended to be used by healthcare professionals in hospital, clinical and field environments.

Source page: https://510kreport.com/device/K023653
Methodology: https://510kreport.com/methodology