www.fdanews.com/articles/88329-bovie-medical-corporation-announces-the-filing-of-an-fda-510-k-application-for-new-gi-device
BOVIE MEDICAL CORPORATION ANNOUNCES THE FILING OF AN FDA 510(K) APPLICATION FOR NEW GI DEVICE
July 12, 2006
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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