WLP SINGLE-SEGMENT VERSION WLP SOLO VII

WLP SINGLE-SEGMENT VERSION WLP SOLO VII is an FDA 510(k)-cleared medical device (K961891) 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.