RODENSTOCK LASER SLITLAMP

RODENSTOCK LASER SLITLAMP is an FDA 510(k)-cleared medical device (K973220) manufactured by G. Rodenstock Instrumente GmbH. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 3, 1997. Regulation: 8.