Regulacje i polityka gospodarcza · 09/10/1996

FDA Approves EDAP Technomed Group's Prostatron for Premarket Approval

The US Food and Drug Administration (FDA) has approved the premarket approval application of EDAP Technomed Group (U.S.A), Inc. for the ProstatronTM, a medical device, following the recommendation of the Gastroenterology and Urology Devices Panel of the Medical Devices Advisory Committee.