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Entreprise · 19/04/19941 min de lecture
Medtronic, Inc.; Premarket Approval of the MedtronicRegister TransveneRegister Lead System
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Résumé
The Food and Drug Administration (FDA) is announcing its approval of the application by Medtronic, Inc., Minneapolis, MN, for premarket approval, under section 515 of the Federal Food, Drug, and Cosmetic Act (the act), of the Medtronic Transvene Lead System. After reviewing the recommendation of the Circulatory System Devices Panel, FDA's Center for Devices and Radiological Health (CDRH) notified the applicant, by letter of December 9, 1993, of the approval of the application.
Langue originale de la source: Federal Register — Health and Human ServicesOuvrir le communiqué original →