# K090089: Belmont Hyperthermia Pump

- Pathway: 510(k) (Special)
- Applicant: Belmont Instrument Corp.
- Decided: Feb 12, 2009 after 29 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices 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.

## Most influential descendants
- K152208: The Belmont Hyperthermia Pump (2015), 0 descendants of its own

## Indications for use
The intended use of the Belmont Hyperthermia Pump is to raise the temperature of the thoracic or peritoneal cavity to the desired target temperature by continuously lavaging the cavity with circulating warmed sterile solution, according to a protocol to be selected by the physician.

Source page: https://510kreport.com/device/K090089
Methodology: https://510kreport.com/methodology