DL900 SERIES HOLTER RECORDER

DL900 SERIES HOLTER RECORDER is an FDA 510(k)-cleared medical device (K071733) manufactured by Braemar, 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 July 23, 2007. Regulation: 8.