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