FDA Approvals - FDA Classifies Voluntary Physician Advisory Letter on Riata and Riata
FDA Classifies Voluntary Physician Advisory Letter on Riata and Riata ST Silicone Defibrillation Leads as Class I ...
St. Jude Medical, Inc. , a global medical device company, today announced that the U.S. Food and Drug Administration has classified its voluntary medical device advisory letter to physicians from Nov.
FDA approves modernized labeling for ViroPharma's Vancocin Capsules
ViroPharma Incorporated today announced the modernization of labeling for Vancocin (vancomycin hydrochloride, USP) Capsules made effective through the U.S. Food and Drug Administration's (FDA) approval of a supplemental new drug application.