
Wright Linear Pump, Inc.
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WRIGHT MODEL 51 AND 52 SEQUENTIAL COMPRESSION SYSTEMS is an FDA 510(k)-cleared medical device (K071040) manufactured by Wright Linear Pump, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 21, 2007. Regulation: 8.