SHEA'S EAR SPECULUM HOLDER PORT MANNS

SHEA'S EAR SPECULUM HOLDER PORT MANNS is an FDA 510(k)-cleared medical device (K822011) manufactured by Kelleher Corp.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 11, 1982. Regulation: 8.