
Sonosite,Inc.
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SONOSITE MICROMAXX DIAGNOSTIC ULTRASOUND SYSTEM (C3 SERIES) is an FDA 510(k)-cleared medical device (K053069) manufactured by Sonosite,Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 15, 2005. Regulation: 8.