PROVIEW EYE PRESSURE MONITOR

PROVIEW EYE PRESSURE MONITOR is an FDA 510(k)-cleared medical device (K011199) manufactured by Bausch & Lomb, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 1, 2001. Regulation: 8.