I/A VITROPHAGE MODEL YPR 2001

I/A VITROPHAGE MODEL YPR 2001 is an FDA 510(k)-cleared medical device (K904909) manufactured by Visioncare Devices, 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 January 27, 1991. Regulation: 8.