
Usgi Medical
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G-PROX ENDOSCOPIC GRASPER, MODEL 205333 is an FDA 510(k)-cleared medical device (K093018) manufactured by Usgi Medical. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 6, 2009. Regulation: 8.