# K203803: VASOBand Vascular Compression Device

- Pathway: 510(k) (Traditional)
- Applicant: Vasoinnovations, Inc.
- Decided: Jan 26, 2021 after 29 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: 2 generations back to K070423 (2007). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K190318: VASOBand Vascular Compression Device, Vasoinnovations, Inc. (2019) Summary page 4.

## Indications for use
The VASOBandTM is a compression device to assist patent hemostasis of the radial artery after a transradial procedure.

Source page: https://510kreport.com/device/K203803
Methodology: https://510kreport.com/methodology