Smiths Medical Receives FDA 510(k) Clearance for ViaValve Safety IV Catheter

Smiths Medical has announced its ViaValve safety IV catheter has received FDA 510(k) clearance, according to a news release.

 

The ViaValve catheter is designed to help reduce the risk of infection and cross contamination caused by blood exposure during IV starts, according to the company.

 

It will be available for sale by the end of this summer.

 

Smiths Medical is based in St. Paul, Minn.

 

Related Articles on FDA Clearances:

ActiViews Receives FDA 510(k) Clearance of CT-Guide Needle Guidance System for Liver Interventions

Abbott Receives FDA Clearance for Use of Femtosecond Laser for Arcuate Incisions

CurveBeam Receives FDA 510(k) Approval for the pedCAT 3D Foot and Ankle Scanner

Copyright © 2024 Becker's Healthcare. All Rights Reserved. Privacy Policy. Cookie Policy. Linking and Reprinting Policy.

 

Featured Webinars

Featured Whitepapers