この記事の翻訳を準備しています。それまでの間、英語の原文を表示します。
ビジネス · 1994/4/191 分で読めます
Medtronic, Inc.; Premarket Approval of the MedtronicRegister TransveneRegister Lead System
ローカル自動翻訳 · 情報源の原言語
概要
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.
情報源の原言語: Federal Register — Health and Human Services原文の発表を開く →