# K871271: Huntleigh Flowpress AC300 Pump, SQ301/302/320 Gar.

- Pathway: 510(k) (Traditional)
- Applicant: Huntleigh Technology, Inc.
- Decided: Sep 15, 1987 after 168 days
- Product code: DRM (Compressor, Cardiac, External)
- Device class: 2
- Regulation: 21 CFR 870.5200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K961292: WLP Sequential Version Model WLP Solo VI, WLP Solo Sequential (1996), 2 descendants of its own
- K071040: Wright Model 51 and 52 Sequential Compression Systems (2007), 1 descendant of its own
- K131387: Wright Gradient 52 - Torso (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K871271
Methodology: https://510kreport.com/methodology