DATASCOPE INTERLOCK GUIDE WIRE EXTENSION

DATASCOPE INTERLOCK GUIDE WIRE EXTENSION is an FDA 510(k)-cleared medical device (K894318) manufactured by Datascope Corp.. 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 11, 1989. Regulation: 8.