# K222182: Radial Artery Compression Tourniquets

- Pathway: 510(k) (Traditional)
- Applicant: Beijing Demax Medical Technology Co.,Ltd
- Decided: Jan 4, 2023 after 166 days
- Product code: DXC (Clamp, Vascular)
- Device class: 2
- Regulation: 21 CFR 870.4450
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K232577: Radial Compression Device (2024), 0 descendants of its own

## Indications for use
The Radial Artery Compression Tourniquet is designed for temporary hemostasis of radial artery post percutaneous puncture.

Source page: https://510kreport.com/device/K222182
Methodology: https://510kreport.com/methodology