MINI-LOGGER SERIES 2000

MINI-LOGGER SERIES 2000 is an FDA 510(k)-cleared medical device (K991045) manufactured by Mini-Mitter Co., Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 20, 1999. Regulation: 8.