# K022753: Reprocesses Used Disposable Sequential Compression Sleeves/Wraps

- Pathway: 510(k) (Traditional)
- Applicant: Medical Device Services
- Decided: Nov 14, 2002 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Indications for use
Sequential compression sleeves are intended to increase venous return from the lower extremities as a prophylaxis for the formation of deep vein thrombosis or pulmonary embolism in non ambulatory patients. Sequential compression sleeves are single patient use devices only.

Source page: https://510kreport.com/device/K022753
Methodology: https://510kreport.com/methodology