
Imm Enterprises , Ltd.
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H.R. JAKOBI SURG. INSTR. #10 34/36 is an FDA 510(k)-cleared medical device (K834178) manufactured by Imm Enterprises , Ltd.. This device is classified under the Neurology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 22, 1984. Regulation: 8.

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