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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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