# K131193: Actitouch Act-Adaptive Compression Therapy System

- Pathway: 510(k) (Traditional)
- Applicant: Tactile Systems Technology, Inc.
- Decided: Jun 18, 2013 after 53 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 K882683 (1988). 1 ancestor in all.
2 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K882683: Jobst Extremity Pump (R) System 7500, Jobst Institute, Inc. (1988) Summary page 1.

## Most influential descendants
- K200353: ManaFlow (2020), 1 descendant of its own
- K240011: Lymphedema Compression (2024), 0 descendants of its own

## Indications for use
The ACTitouch™ Adaptive Compression Therapy system provides graduated compression in both sustained and intermittent settings for use in: Enhancing venous return Reducing venous leg ulcer healing time Treatment and promotion of healing of stasis dermatitis and venous stasis ulcers Treatment of chronic venous insufficiency Reducing edema due to venous stasis Treatment of lymphedema

Source page: https://510kreport.com/device/K131193
Methodology: https://510kreport.com/methodology