# K073013: CTU676 Device

- Pathway: 510(k) (Traditional)
- Applicant: Compression Technologies Unlimited, Inc.
- Decided: Nov 21, 2007 after 27 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) TravelAir™: named in the summary without a submission number
- (no number) DVTcare™ CA5: named in the summary without a submission number
- (no number) WizAir™: named in the summary without a submission number

## Indications for use
The CTU676 is a prescriptive device that includes continuous enhanced circulation therapy of the lower limbs. The CTU676 is intended for use in the following: * Enhancing blood circulation * Reducing wound-healing time. * Preventing Deep Vein Thrombosis (DVT). * Diminishing post-operative pain and swelling · Treatment and assistance in healing: stasis dermatitis * Venous stasis ulcers; arterial and diabetic ulcers * Treatment of Chronic venous insufficiency * Reducing edema

Source page: https://510kreport.com/device/K073013
Methodology: https://510kreport.com/methodology