RODENSTOCK SLITLAMP (MODEL 5000 & 4000)

RODENSTOCK SLITLAMP (MODEL 5000 & 4000) is an FDA 510(k)-cleared medical device (K962532) manufactured by Expertech Assoc., 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 July 24, 1996. Regulation: 8.