IOLAB/SITE PERISTALTIC MODULE

IOLAB/SITE PERISTALTIC MODULE is an FDA 510(k)-cleared medical device (K944995) 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 October 4, 1995. Regulation: 8.