FLEXON TEMPORARY CARDIAC PACER LEAD

FLEXON TEMPORARY CARDIAC PACER LEAD is an FDA 510(k)-cleared medical device (K955722) 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 March 14, 1996. Regulation: 8.