RENU MULTIPLUS LUBRICATING & REWETTING DROPS

RENU MULTIPLUS LUBRICATING & REWETTING DROPS is an FDA 510(k)-cleared medical device (K980591) 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 June 23, 1998. Regulation: 8.