PRELUDEEASE HYDROPHILIC SHEATH INTRODUCER

PRELUDEEASE HYDROPHILIC SHEATH INTRODUCER is an FDA 510(k)-cleared medical device (K140543) manufactured by Merit Medical Systems, 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 October 15, 2014. Regulation: 8.