MS AMPLATZ EXTRA STIFF GUIDE WIRE

MS AMPLATZ EXTRA STIFF GUIDE WIRE is an FDA 510(k)-cleared medical device (K942382) manufactured by Meadox Surgimed, 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 August 21, 1994. Regulation: 8.