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Réglementation et droit · 08/10/19961 min de lecture
Medtronic, Inc.; Premarket Approval of the CapSureFixRegister Pacing Lead, Model 4068
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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 the Federal Food, Drug, and Cosmetic Act (the act), of the CapSureFix Pacing Lead, Model 4068. FDA's Center for Devices and Radiological Health (CDRH) notified the applicant, by letter of March 29, 1996, of the approval of the application.
Langue originale de la source: Federal Register — All DocumentsOuvrir le communiqué original →