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Vermont Medical, Inc.
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NEUROPLUS, MODEL A10040, A10041, A10042, A10043 is an FDA 510(k)-cleared medical device (K010638) manufactured by Vermont Medical, 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 May 2, 2001. Regulation: 8.