MENTOR GEMINI HEMOSTATIC ERASER

MENTOR GEMINI HEMOSTATIC ERASER is an FDA 510(k)-cleared medical device (K971538) manufactured by Mentor Ophthalmics, 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 July 13, 1997. Regulation: 8.