MEDILOG 9000-II AMBULATORY RECORDER

MEDILOG 9000-II AMBULATORY RECORDER is an FDA 510(k)-cleared medical device (K890647) 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 March 14, 1989. Regulation: 8.