PHILIPS EASYGUIDE NEURO

PHILIPS EASYGUIDE NEURO is an FDA 510(k)-cleared medical device (K961834) manufactured by Philips Medical Systems, 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 November 7, 1996. Regulation: 8.