# K953953: Deroyal Industries, Inc. Pneumatic Tourniquet Cuff

- Pathway: 510(k) (Traditional)
- Applicant: Deroyal Industries, Inc.
- Decided: Sep 29, 1995 after 38 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
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K112874: EZ Vein Inflatable Tourniquet (2011), 1 descendant of its own
- K162365: T-Cuff (2017), 0 descendants of its own

Source page: https://510kreport.com/device/K953953
Methodology: https://510kreport.com/methodology