
Surgi-Quip Inc.U
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SELF-CONTAINED MOBILE OPHTHAL. OPER. . is an FDA 510(k)-cleared medical device (K822427) manufactured by Surgi-Quip Inc.U. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 13, 1982. Regulation: 8.