KOGAN ENDOSPECULUM 9-1/2

KOGAN ENDOSPECULUM 9-1/2 is an FDA 510(k)-cleared medical device (K842111) manufactured by J. Sklar Mfg. Co., 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 18, 1984. Regulation: 8.