WLP GRADIENT SEQUENTIAL VERSION/WLP PROLITE/WLP WLP-II LITE

WLP GRADIENT SEQUENTIAL VERSION/WLP PROLITE/WLP WLP-II LITE is an FDA 510(k)-cleared medical device (K961797) 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 November 5, 1996. Regulation: 8.