OMNISORB II, NONWOVEN SPONGE, STERILE AND NON

OMNISORB II, NONWOVEN SPONGE, STERILE AND NON is an FDA 510(k)-cleared medical device (K931610) manufactured by Omni Mfg., Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 23, 1993. Regulation: 8.