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# Access Vascular Midline Catheter Cleared
- URL: https://www.fdaweb.com/access-vascular-midline-catheter-cleared/
- Published: 2021-02-11T12:00:00.000Z
- Updated: 2026-09-14T16:46:31.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5148642

FDA has cleared an Access Vascular 510(k) for its HydroMID midline catheter, which is made using the company’s proprietary biomaterial that it says has been shown to reduce thrombus accumulation by up to 97% when compared to standard polyurethane catheters. HydroMID is described as a 4 French, single lumen, midline catheter with a maximum usable length of 20cm. Midlines are intended for use for up to 30 days, the company says.