FDA Sets Regulatory Review Period for TriReme Medical's Chocolate Touch Drug-Coated Balloon Catheter
July 07, 2025
July 07, 2025
WASHINGTON, July 7 (TNSFR) -- The U.S. Department of Health and Human Services Food and Drug Administration has determined the regulatory review period for the Chocolate Touch, a Paclitaxel drug coated percutaneous transluminal angioplasty balloon catheter developed by TriReme Medical LLC.
This device, designed for PTA of femoral or popliteal arteries, underwent a rigorous review process before earning FDA approval for commercial use.
According to the notice published i . . .
This device, designed for PTA of femoral or popliteal arteries, underwent a rigorous review process before earning FDA approval for commercial use.
According to the notice published i . . .