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Zdrowie i gospodarka · 15/02/2006

FDA Classifies Implantable Intra-Aneurysm Pressure Measurement System as Class II Device

The FDA has classified the implantable intra-aneurysm pressure measurement system as a Class II device, requiring special controls to ensure its safety and effectiveness, and has made a guidance document available to support this classification.

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