# K102582: Arterioflow Model 7500 Sequential Compression Device

- Pathway: 510(k) (Traditional)
- Applicant: Devon Medical, Inc.
- Decided: Oct 7, 2010 after 29 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 K881632 (1988). 13 ancestors in all.
No later device cites it as a predicate yet.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K101523: Circuflow 5200 Sequential Compression Device, Devon Medical, Inc. (2010) Summary page 1.
- K072666: Bioarterial Plus, Arterial Blood Flow Enhancement System, Bio Compression Systems, Inc. (2007). Our reading of the summary gave K072660, FDA’s number for Endure Implant, Model 5108, 5111, 5113, 5114 (Imtec Corp.). Corrected to the number one digit away whose FDA name carries the summary’s words for the device, “BioArterial Plus”.

## Indications for use
The ArterioFlow 7500 is intended as an adjunctive therapy for patients with ischemic disease of the lower extremities, due to one or more of the following causes: * Amputations (minor) * Angioplasty/stent failure * Arteriopathic wounds * Graft failure * Intermittent claudication * Ischemia * Night Pain * Rest Pain * Small vessel disease * Ulcers The device is intended for home and hospital use.

Source page: https://510kreport.com/device/K102582
Methodology: https://510kreport.com/methodology