# K031722: Jsa Reprocessed Compression Sleeve Devices

- Pathway: 510(k) (Traditional)
- Applicant: Jack Speer and Assoc., Inc.
- Decided: Nov 25, 2003 after 175 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 K890938 (1989). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K890938: Kendall SCD Therapeutic System, Kendall Healthcare Products Co. Div.Of Tyco Health (1989) Summary page 1.

## Cited in the summary but kept off the family tree
- K946646: Kendall Compression Sleeve Devices. Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree

## Indications for use
These devices are designed to increase blood flow in the non-ambulatory patient in order to prevent deep vein thromboses or pulmonary embolism.

Source page: https://510kreport.com/device/K031722
Methodology: https://510kreport.com/methodology