Home » 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.
Genetic
Engineering News
KEYWORDS FDAnews Device Daily Bulletin
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