BioScan’s LightWire Nears FDA, European Submissions
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Health/Technology on 08 17th, 2009 |
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BioScan Technologies , a Yokneam, Israel firm developing a 0.014″ intravascular ultrasound guidewire for coronary and peripheral procedures, is planning to file a 510(k) submission to the FDA in the next two months, Medgadget has learned. Furthermore, the company expects to complete the CE Mark...