# K042217: Flowmedic, Model 220

- Pathway: 510(k) (Traditional)
- Applicant: Flowmedic (Israel), Ltd.
- Decided: Jan 12, 2005 after 149 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: 1 generation back to K942530 (1996). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K024019: Arterialflow System, Model 32A, Aircast, Inc. (2003) Summary page 3.
- K942530: Art-Assist Model AA-1000, Aci Medical, Inc. (1996) Summary page 3.
- K012994: Wizair DVT, Medical Compression Systems (Dbn), Ltd. (2002) Summary page 3.

## Indications for use
The FlowMedicTM FM220 System is intended for the improvement of blood circulation in the lower extremities to help prevent and reduce complications of poor circulation.

Source page: https://510kreport.com/device/K042217
Methodology: https://510kreport.com/methodology