STORZ E8010 ERGOTEC/PREMIERE ADAPTOR

STORZ E8010 ERGOTEC/PREMIERE ADAPTOR is an FDA 510(k)-cleared medical device (K964743) manufactured by Storz Instrument 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 February 2, 1997. Regulation: 8.