HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBE

HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBE is an FDA 510(k)-cleared medical device (K931072) manufactured by Hgm, 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 November 9, 1994. Regulation: 8.