BAUSCH & LOMB FREQUENT REPLACEMENT CASE SYSTEM

BAUSCH & LOMB FREQUENT REPLACEMENT CASE SYSTEM is an FDA 510(k)-cleared medical device (K896685) 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 December 25, 1989. Regulation: 8.