FLEXON TEMPORARY CARDIAC CONDUCTIVE MULTIFILAMENT

FLEXON TEMPORARY CARDIAC CONDUCTIVE MULTIFILAMENT is an FDA 510(k)-cleared medical device (K855139) manufactured by Davis & Geck, 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 February 25, 1986. Regulation: 8.