Zdrowie i gospodarka · 30/10/2000

FDA Corrects Premarket Approval Requirement for Urinary Continence Device

The FDA is correcting a final rule from 2000 that incorrectly stated the effective date for a premarket approval application for an implanted mechanical/hydraulic urinary continence device, intended to treat urinary incontinence.

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

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