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Drager Medizintechnik GmbH
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SOLA 700,SOLA 500, SOLA 300 is an FDA 510(k)-cleared medical device (K010724) manufactured by Drager Medizintechnik GmbH. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 6, 2001. Regulation: 8.