FDA 510(k) Applications Submitted by KLS MARTIN GMBH + CO. KG

FDA 510(k) Number Submission Date Device Name Applicant
K081678 06/17/2008 CONMED BEAMER SYSTEM C600 KLS MARTIN GMBH + CO. KG
K183526 12/19/2018 Codman Electrosurgical Generator, Foot Pedal KLS Martin GmbH + Co. KG


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