# K003828: Vaso Press DVT Foot Garment #VP 520

- Pathway: 510(k) (Traditional)
- Applicant: Britt Corp., Inc.
- Decided: May 18, 2001 after 158 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.
5 later devices descend from it; 3 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- 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
- K253386: DVT Garment (2026), 0 descendants of its own
- K122179: Vasopress DVT Leg Garments (Sterile) Vasopress DVT Foot Garments (Sterile) (2012), 0 descendants of its own
- K052691: Suretek Medical Reprocessed Compression Sleeves (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K003828
Methodology: https://510kreport.com/methodology