
Carl Zeiss, Inc.
Free shipping on orders over $99 · 30-day returns
ZEISS VISULAS ARGON LASER is an FDA 510(k)-cleared medical device (K923341) manufactured by Carl Zeiss, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 27, 1992. Regulation: 8.