# K991038: Vaso Press DVT System, Models VP500, VP501

- Pathway: 510(k) (Traditional)
- Applicant: Britt Corp., Inc.
- Decided: Jun 22, 2000 after 451 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.
13 later devices descend from it; 4 cite it directly.
0 of 14 devices 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.

## Most influential descendants
- K090308: Restep Dvy System, Model RSP-101 (2009), 8 descendants of its own
- K130571: Devon Cirona 6100 DVT (2013), 6 descendants of its own
- K141578: Devon Cirona 6200 DVT (2014), 4 descendants of its own
- K112838: Vasopress Reprocessed DVT Leg / Foot Garments (2011), 3 descendants of its own
- K201547: B&J DVT Foot Garments, Models 820 Series (2020), 1 descendant of its own

## Indications for use
The Vaso Press system is an external pneumatic compression system intended to lower the risk of deep vein thrombosis (DVT) in patients whom may be at risk

Source page: https://510kreport.com/device/K991038
Methodology: https://510kreport.com/methodology