# K024074: Reprocessed Compression Sleeves

- Pathway: 510(k) (Traditional)
- Applicant: Alliance Medical Corp.
- Decided: Mar 7, 2003 after 87 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
Longest line of descent: 1 generation back to K961405 (1996). 1 ancestor in all.
1 later device descends 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)
- K961405: Alba Health Pas Wrap System, Alba-Waldensian, Inc. (1996) Summary page 2.

## Most influential descendants
- K100909: Reprocessed Compression Sleeves (2010), 0 descendants of its own

## Indications for use
Reprocessed Compression Sleeves are indicated for use in providing external compression therapy to reduce the incidence of deep vein thrombosis and resulting pulmonary embolism in patients at risk for thrombosis formation.

Source page: https://510kreport.com/device/K024074
Methodology: https://510kreport.com/methodology