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Negócios · 22/07/19941 min de leitura
Grieshaber & Co., Inc.; Premarket Approval of Grieshaber Scleral Buckling Balloon Catheter
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Resumo
The Food and Drug Administration (FDA) is announcing its approval of the application by Grieshaber & Co., Inc., Kennesaw, GA, for premarket approval, under section 515 of the Federal Food, Drug, and Cosmetic Act (the act), of Grieshaber Scleral Buckling Balloon Catheter. FDA's Center for Devices and Radiological Health (CDRH) notified the applicant, by letter of June 2, 1994, of the approval of the application.
Idioma original da fonte: Federal Register — Health and Human ServicesAbrir o comunicado original →