ZEISS 30 SL-L

ZEISS 30 SL-L is an FDA 510(k)-cleared medical device (K862004) manufactured by Carl Zeiss, 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 June 16, 1986. Regulation: 8.