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Viasys Healthcare GmbH
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MASTERSCREEN PNEUMO & MASTERSCOPE is an FDA 510(k)-cleared medical device (K071753) manufactured by Viasys Healthcare GmbH. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 13, 2007. Regulation: 8.