# K121718: A-V Foot Pump

- Pathway: 510(k) (Traditional)
- Applicant: Dalian Labtek Science & Development Co., Ltd.
- Decided: Aug 17, 2012 after 67 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
A-V Hand & Foot Pump, Model LBTK-M-l 1000, is intended for use to enhance blood circulation in the arteries and veins in patents. The indications vary depending on whether pump is used with the foot pad or hand pad. A. Foot use - Acute Edema - Chronic Edema - Circulation Enhancement - Deep Vein Thrombosis and Pulmonary Embolism Prophylaxis - Leg Pain Incident to Trauma or Surgery - Leg Ulcers - Venous Stasis/Venous Insufficiency B. Hand use - Acute Edema - Chronic Edema - Circulation Enhancement - Pain Incident to Trauma or Surgery

Source page: https://510kreport.com/device/K121718
Methodology: https://510kreport.com/methodology