URAM OPHTHALMIC LASER ENDOSCOPE

URAM OPHTHALMIC LASER ENDOSCOPE is an FDA 510(k)-cleared medical device (K910532) manufactured by Martin S. Knopf 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 May 27, 1991. Regulation: 8.