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Entreprise · 22/07/19941 min de lecture
Grieshaber & Co., Inc.; Premarket Approval of Grieshaber Scleral Buckling Balloon Catheter
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Résumé
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.
Langue originale de la source: Federal Register — Health and Human ServicesOuvrir le communiqué original →