
Imm Enterprises , Ltd.
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JAKOBI SURG. INSTRUMENTS #7 44/47 is an FDA 510(k)-cleared medical device (K834189) 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 March 5, 1984. Regulation: 8.