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Date: 2012-04-23 00:34:29Technology Food law Pharmaceuticals policy Medical equipment Medical device Medical technology Premarket approval Federal Food Drug and Cosmetic Act Center for Devices and Radiological Health Medicine Food and Drug Administration Health | MAR[removed]Pierre Fabre MEDICAL DEVICES 510(K) SUMMARYAdd to Reading ListSource URL: www.accessdata.fda.govDownload Document from Source WebsiteFile Size: 135,02 KBShare Document on Facebook |