# K171215: QiF Blood and Fluid Warmer

- Pathway: 510(k) (Traditional)
- Applicant: Quality IN Flow, Ltd.
- Decided: Sep 27, 2017 after 155 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K180154: QiF Blood and Fluid Warmer (2018), 1 descendant of its own
- K211800: Warrior Blood and Fluid Warmer, Warrior EXTREME Blood and Fluid Warmer, Warrior Lite Blood and Fluid Warmer (2022), 0 descendants of its own

Source page: https://510kreport.com/device/K171215
Methodology: https://510kreport.com/methodology