Bovie Medical Corporation Announces Filing Of An FDA 510(K) Application For New GI Device

MELVILLE, N.Y.--(BUSINESS WIRE)--July 12, 2006--Bovie Medical Corporation (the "Company") (Amex: BVX - News), 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.
MORE ON THIS TOPIC