VISULINK 900 ARGON

VISULINK 900 ARGON is an FDA 510(k)-cleared medical device (K952894) manufactured by Carl Zeiss, 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 August 13, 1995. Regulation: 8.