# K112874: EZ Vein Inflatable Tourniquet

- Pathway: 510(k) (Traditional)
- Applicant: Dominion Medical Devices, LLC
- Decided: Oct 17, 2011 after 17 days
- Product code: KCY (Tourniquet, Pneumatic)
- Device class: 1
- Regulation: 21 CFR 878.5910
- 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 K875092 (1988). 2 ancestors in all.
1 later device descends 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)
- K875092: Degania Silicone Tourniquet, Degania Silicone, Ltd. (1988) Summary page 1.
- K953953: Deroyal Industries, Inc. Pneumatic Tourniquet Cuff, Deroyal Industries, Inc. (1995) Summary page 1.

## Most influential descendants
- K162365: T-Cuff (2017), 0 descendants of its own

## Indications for use
The EZvein inflatable secondary tourniquet is used in conjunction with a non-pneumatic tourniquet, to enhance the presentation of veins for access (blood draw or IV administration.)

Source page: https://510kreport.com/device/K112874
Methodology: https://510kreport.com/methodology