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 · 1997/6/181 分で読めます
Gen-ProbeRegister, Inc.; Premarket Approval of Gen- ProbeRegister Amplified Mycobacterium Tuberculosis Direct Test
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 Gen-Probe , Inc., San Diego, CA, for premarket approval, under the Federal Food, Drug, and Cosmetic Act (the act), of the Gen-Probe Amplified Mycobacterium tuberculosis Direct Test (MTD). After reviewing the recommendation of the Microbiology Devices Panel, FDA's Center for Devices and Radiological Health (CDRH) notified the applicant, by letter on December 15, 1995, of the approval of the application.
情報源の原言語: Federal Register — Food and Drug Administration原文の発表を開く →