GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP

GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP is an FDA 510(k)-cleared medical device (K897119) manufactured by Grieshaber & 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 April 11, 1990. Regulation: 8.