# K060220: PBS Model 701A Compression Therapy Device

- Pathway: 510(k) (Special)
- Applicant: Mego Afek
- Decided: Feb 9, 2006 after 10 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.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K103247: Vascucomp (2010), 0 descendants of its own
- K072372: Phlebopress Model 601A Compression Therapy Device (2007), 0 descendants of its own

## Indications for use
Treatment of Venous disorders and Dysfunction of the "Muscle Pump"

Source page: https://510kreport.com/device/K060220
Methodology: https://510kreport.com/methodology