H.R. JAKOBI SURG. INSTRU. SECT. 48

H.R. JAKOBI SURG. INSTRU. SECT. 48 is an FDA 510(k)-cleared medical device (K834542) manufactured by Imm Enterprises , Ltd.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 26, 1984. Regulation: 8.