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# FDA Clears Teleflex Arrow Midline Antimicrobial Catheter
- URL: https://www.fdaweb.com/fda-clears-teleflex-arrow-midline-antimicrobial-catheter/
- Published: 2016-10-17T12:00:00.000Z
- Updated: 2026-09-14T21:40:02.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5137091

FDA has cleared a Teleflex 510(k) to market its Arrow Midline with Chlorag+ard Technology, an anti-thrombogenic and antimicrobial peripheral venous catheter designed to minimize common midline catheter complications such as catheter intraluminal occlusion, thrombus accumulation and microbial colonization on the catheter surface for a minimum of 30 days. The devices are also designed for use with high-pressure injection for diagnostic studies, according to the company. They will be packaged sterile in kits that will include components to facilitate insertion, the company says.