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Zdrowie i gospodarka · 30/04/2026

FDA Classifies Laser-Powered Inferior Vena Cava Filter Retrieval Catheter as Class II Device

The FDA has classified the laser-powered inferior vena cava filter retrieval catheter as a Class II device, subject to special controls, to ensure its safety and effectiveness while reducing regulatory burdens and enhancing patient access to innovative devices.

Source: Federal Register — Food and Drug AdministrationOpen original release →