# K122873: Vasopouse Deep Vein Thrombosis Compression Device Model Ipcs, Model SQS

- Pathway: 510(k) (Special)
- Applicant: Caremed Supply, Inc.
- Decided: Jan 15, 2013 after 118 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: 3 generations back to K953648 (1996). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110977: Vesoflow, Caremed Supply, Inc. (2011) Summary page 1.

## Indications for use
The Caremed Supply Inc. VASOPOUSE® SQS and IPCS Deep Vein Thrombosis (DVT) Compression Devices are intended to increase venous blood flow in at risk patients in order to help prevent deep vein thrombosis.

Source page: https://510kreport.com/device/K122873
Methodology: https://510kreport.com/methodology