PHAKO SYSTEMS VIA 2000

PHAKO SYSTEMS VIA 2000 is an FDA 510(k)-cleared medical device (K833642) manufactured by Pharosystems, 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 March 4, 1984. Regulation: 8.