Avalon gets OK to distribute three new medical devices

January 16, 2009

Avalon Laboratories has just received 510(k) clearances from the U.S. Food and Drug Administration, as well as CE Mark acceptance from the European Union, for three of its new catheter devices. The FDA clearances and E.U. acceptance allowed Avalon to immediately begin distributing the devices to hospitals and health care systems domestically and in the European Union. The new medical device products are marketed under the names Avalon Elite Bi-Caval Dual Lumen Catheter, the Avalon Elite Multi-Port Venous Femoral Catheter and the Avalon Elite Vascular Access Kit.

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