MANAN GWI GUIDE WIRE INTRODUCER

MANAN GWI GUIDE WIRE INTRODUCER is an FDA 510(k)-cleared medical device (K974745) manufactured by Medical Device Technologies, 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 April 5, 1998. Regulation: 8.