# K141360: Tripleplay Pro

- Pathway: 510(k) (Special)
- Applicant: Wildcat Medical, Inc.
- Decided: Jun 12, 2014 after 20 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 no predicate by number.

## Indications for use
TriplePlay Pro (supplied with a pair of model TP-3333, TP-3636, or TP-3434 “cuffs”) is indicated for being an easy to use portable system, prescribed by a physician, to help prevent the onset of DVT in patients by stimulating blood flow in the extremities (simulating muscle contractions). This device can be used to: * Aid in the prevention of DVT; * Enhance blood circulation; * Diminish post-operative pain and swelling; * Reduce wound healing time; * Aid in the treatment and healing of stasis dermatitis, venous stasis ulcers, arterial and diabetic leg ulcers, chronic venous insufficiency and reduction of edema in the lower limbs; * As a prophylaxis for DVT by persons expecting to be stationary for long periods of time

Source page: https://510kreport.com/device/K141360
Methodology: https://510kreport.com/methodology