JAKOBI SURGICAL INSTRUMENTS #3 17/18/19

JAKOBI SURGICAL INSTRUMENTS #3 17/18/19 is an FDA 510(k)-cleared medical device (K834191) manufactured by Imm Enterprises , Ltd.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 21, 1984. Regulation: 8.