VISITEC MICRO-SPONGE SPEARS

VISITEC MICRO-SPONGE SPEARS is an FDA 510(k)-cleared medical device (K896705) manufactured by Visitec Co.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 10, 1990. Regulation: 8.