Zdrowie i gospodarka · 18/05/2000
FDA Classifies Preamendments Female Condom as Class III Device
The FDA is reclassifying the preamendments female condom, intended for contraceptive and prophylactic purposes, as a Class III device requiring premarket approval, under the Federal Food, Drug, and Cosmetic Act and its amendments.
Source: Federal Register — Food and Drug AdministrationOpen original release →