
Hgm, Inc.
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HGM ASPIRATING ENDOOCULAR(TM) PROBE is an FDA 510(k)-cleared medical device (K925663) 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 August 16, 1993. Regulation: 8.

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