# K232577: Radial Compression Device

- Pathway: 510(k) (Traditional)
- Applicant: Ningbo Dizegens Medical Science Co.,Ltd
- Decided: Jan 18, 2024 after 146 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
Longest line of descent: 1 generation back to K222182 (2023). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K222182: Radial Artery Compression Tourniquets, Beijing Demax Medical Technology Co.,Ltd (2023) Summary page 5.

## Indications for use
The radial compression device is designed to apply compression in order to achieve temporary hemostasis of the radial artery after a percutaneous transradial procedure.

Source page: https://510kreport.com/device/K232577
Methodology: https://510kreport.com/methodology