MEDILOG 6000-FD REPORT GENERATOR

MEDILOG 6000-FD REPORT GENERATOR is an FDA 510(k)-cleared medical device (K890330) manufactured by Oxford Medilog, 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 19, 1989. Regulation: 8.