CUTTER, VITREOUS ANTERIOR VITRECTOMY PROBE (AVP)

CUTTER, VITREOUS ANTERIOR VITRECTOMY PROBE (AVP) is an FDA 510(k)-cleared medical device (K950852) manufactured by H.S. Intl. Co., 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 May 18, 1995. Regulation: 8.