ABT12 multi-purpose solution

ABT12 multi-purpose solution is an FDA 510(k)-cleared medical device (K202932) manufactured by Bausch & Lomb, Incorporated. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 27, 2021. Regulation: 8.