# K071744: Aviafit Pulsating Legband

- Pathway: 510(k) (Traditional)
- Applicant: Flowmedic, Ltd.
- Decided: Sep 25, 2007 after 90 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.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K111720: Aviafit (2011), 0 descendants of its own

## Indications for use
The Aviafit T M is intended to improve blood circulation in the lower limbs and reduce the risk of deep vein thrombosis, edema and leg discomfort during limited mobility conditions at home, at the office and during mid-long haul flights.

Source page: https://510kreport.com/device/K071744
Methodology: https://510kreport.com/methodology