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Home » Becton Dickinson’s Hemodialysis Catheter Gets FDA 510(k) Clearance
Becton Dickinson’s Hemodialysis Catheter Gets FDA 510(k) Clearance
The FDA has granted 510(k) clearance to Becton Dickinson’s Pristine Long-Term Hemodialysis Catheter, a device designed to address complications that can cause obstructions and impact performance.
The Pristine catheter has a tip designed to avoid potential complications, including positional occlusion, high recirculation rates and thrombus formation.
The device features a side-hole free tip that minimizes blood-clot adhesion that sometimes occurs when using side-hole catheters and supports blood-clot removal prior to hemodialysis.
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