HGM ILLUMINATING IMAGING ENDOCULAR PROBE

HGM ILLUMINATING IMAGING ENDOCULAR PROBE is an FDA 510(k)-cleared medical device (K931784) 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 February 28, 1994. Regulation: 8.