Sanovas files 510(k) clearance for lung catheter device

01/20/2013 | MassDevice.com (Boston)

Sanovas has submitted an FDA application for a 510(k) clearance to market its Vas Zeppelin Smart Catheter, which is used for the diagnosis and treatment of lung cancer and chronic pulmonary conditions. The move is part of the company's three-pronged strategy to pursue FDA OKs for its more than 37 devices and six product lines.

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