# K024327: Setpoint Endovascular Temperature Probe

- Pathway: 510(k) (Traditional)
- Applicant: Radiant Medical
- Decided: Mar 25, 2003 after 89 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K811742 (1981). 8 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K012512: Setpoint Endovascular Temperature Management System, Radiant Medical (2002) Summary page 2.
- K904404: Multi-Lumen Central Venous Catheter Set, Arrow Intl., Inc. (1991) Summary page 1.

## Most influential descendants
- K042388: Radiant Medical Endocatheter Temperature Probe (2004), 0 descendants of its own

## Indications for use
The SetPoint Endovascular Temperature Probe is indicated for use with the SetPoint Endovascular Temperature Management System to measure core body temperature.

Source page: https://510kreport.com/device/K024327
Methodology: https://510kreport.com/methodology