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Objectivision Pty , Ltd.
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ACCUMAP AUTOMATIC PERIMETER is an FDA 510(k)-cleared medical device (K022304) manufactured by Objectivision Pty , Ltd.. 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 13, 2003. Regulation: 8.