# K090508: The Belmont Buddy Lite Fluid Warmer

- Pathway: 510(k) (Special)
- Applicant: Belmont Instrument Corp.
- Decided: Mar 26, 2009 after 28 days
- Product code: BSB (Warmer, Blood, Non-Electromagnetic Radiation)
- Device class: 2
- Regulation: 21 CFR 864.9205
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The intended use of the Belmont® buddy liteTM Fluid Warmer is to warm blood, blood products, and intravenous solution prior to administration. It is intended to be used by healthcare professionals in clinical environments to prevent hypothermia.

Source page: https://510kreport.com/device/K090508
Methodology: https://510kreport.com/methodology