KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM

KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM is an FDA 510(k)-cleared medical device (K942664) manufactured by The Kendal Co.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 16, 1995. Regulation: 8.