# K122499: Aircast Venaflow Elite System

- Pathway: 510(k) (Traditional)
- Applicant: Djo, LLC
- Decided: Oct 18, 2012 after 63 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.
1 later device descends from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091700: Aircast Venaflow Elite System, Djo, LLC (2009) Summary page 1.
- K102737: Kendall SCD 700 Sequential Compression Controller, Covidien, LLC (2010) Summary page 1.

## Most influential descendants
- K130722: Aircast Venaflow Elite System (2013), 0 descendants of its own

## Indications for use
Prophyaxis for Deep Vein Thrombosis (DVT) for use in a clinical setting or in the home.

Source page: https://510kreport.com/device/K122499
Methodology: https://510kreport.com/methodology