JAKOBI SURG. INSTRUMENTS #6 50

JAKOBI SURG. INSTRUMENTS #6 50 is an FDA 510(k)-cleared medical device (K834187) manufactured by Imm Enterprises , Ltd.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 4, 1984. Regulation: 8.