MODIFIED SITE MACROBORE PHACO NEEDLE

MODIFIED SITE MACROBORE PHACO NEEDLE is an FDA 510(k)-cleared medical device (K922595) manufactured by Chiron Vision Corp.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 30, 1992. Regulation: 8.