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Codman & Shurtleff, Inc.
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CODMAN VPV SYSTEM, MODEL 82-3192 is an FDA 510(k)-cleared medical device (K050739) manufactured by Codman & Shurtleff, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 17, 2005. Regulation: 8.