# K002287: Wizair Compression System

- Pathway: 510(k) (Special)
- Applicant: Medical Compression Systems (Dbn), Ltd.
- Decided: Aug 25, 2000 after 29 days
- Product code: JOW (Sleeve, Limb, Compressible)
- Device class: 2
- Regulation: 21 CFR 870.5800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
64 later devices descend from it; 4 cite it directly.
0 of 65 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
- K022340: Travelair Portable Compression System (2003), 31 descendants of its own
- K061125: Dvtcare CA5 (2006), 30 descendants of its own
- K060146: Activecare ++ System (2006), 30 descendants of its own
- K103187: Tripleplay-VT Vascular Therapy System (2011), 25 descendants of its own
- K133274: Vena Pro (2014), 22 descendants of its own

Source page: https://510kreport.com/device/K002287
Methodology: https://510kreport.com/methodology