# K890014: Disposable Color-Cuffs

- Pathway: 510(k) (Traditional)
- Applicant: Instrumed, Inc.
- Decided: Jan 24, 1989 after 21 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.
4 later devices descend from it; 1 cites it directly.
0 of 5 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
- K012632: Tourniquet Cuff; Pneumatic Tourniquet (2001), 3 descendants of its own
- K112384: Abdominal Tourniquet System (2011), 2 descendants of its own
- K133029: Abdominal Aortic and Junctional Tourniquet (Aajt) Device (2013), 1 descendant of its own
- K221661: Abdominal Aortic and Junctional Tourniquet - Stabilized (AAJT-S) (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K890014
Methodology: https://510kreport.com/methodology