SCIMED SCEPTOR PTCA GUIDE WIRE

SCIMED SCEPTOR PTCA GUIDE WIRE is an FDA 510(k)-cleared medical device (K950534) manufactured by Scimed Life 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 April 27, 1995. Regulation: 8.