FDAnews Device Daily Bulletin

BOVIE MEDICAL CORPORATION ANNOUNCES THE FILING OF AN FDA 510(K) APPLICATION FOR NEW GI DEVICE

July 13, 2006
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Bovie Medical Corporation, a manufacturer and marketer of electrosurgical products, today announced the filing with the Food and Drug Administration (FDA) of a 510(K) application for an electrosurgical product for the gastroenterological market. The GI device has been designed in conjunction with input from GI surgeons and nurses, offering many features including a touch screen interface, physician preference database, neutral electrode monitoring, and common sense messages.
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