# K801766: Jackson-Pratt Large Vol. Closed Wound

- Pathway: 510(k) (Traditional)
- Applicant: American Heyer Schulte
- Decided: Aug 20, 1980 after 23 days
- Product code: GCY (Apparatus, Suction, Single Patient Use, Portable, Nonpowered)
- Device class: 1
- Regulation: 21 CFR 878.4680
- 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. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K140383: ALLOX2 Tissue Expanders (2014), 1 descendant of its own
- K214124: AlloX2 Pro Tissue Expanders (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K801766
Methodology: https://510kreport.com/methodology