Press Release:
Visualase Inc. Selected to Present at Epilepsy Conference Highlighting New and Promising Epilepsy Therapies. Epilepsy Pipeline Update 2010 to Take Place February 25-26 in San Francisco.
Press Release:
Visualase Inc. Selected to Present at Epilepsy Conference Highlighting New and Promising Epilepsy Therapies. Epilepsy Pipeline Update 2010 to Take Place February 25-26 in San Francisco.
Houston, Texas October 6, 2009. The U.S. FDA granted 510(k) clearance (K092197) for the PhoTex30 Diode Laser Series, Model 980nm, 810nm, 940nm. The PhoTex30 Diode Laser Series, distributed by Visualase, Inc. received broad clearance for use in surgical applications requiring ablation and coagulation of soft tissue including general surgery, urology, neurosurgery, and other surgical specialties.
FDA grants clearance for the Visualase System
Houston, Texas March 1st, 2006 The U.S. FDA granted 510(k) clearance (K053087) for the Visualase Cooled Laser Applicator System. The Visualase Cooled Laser Applicator System, manufactured by BioTex, Inc. and to be distributed by Visualase, Inc. received clearance for marketing with broad use in a number of medical specialties. “This family of products consists of a number of novel advancements in laser applicator systems,” stated Dr. Ashok Gowda, President and CEO of Visualase. “The laser diffusing fiber and cooling catheter system can be used together to allow use of higher laser powers and faster ablation times, while minimizing risk of applicator damage and tissue carbonization,” he added.