FDA 510(k) Applications Submitted by TRUMPF MEDIZIN SYSTEME GMBH + CO. KG

FDA 510(k) Number Submission Date Device Name Applicant
K091246 04/27/2009 ILED 3 MOBILE (I300M), TRULIGHT 5500 MOBILE (T500M), TRULIGHT 5300 MOBILE (T300M) TRUMPF MEDIZIN SYSTEME GMBH + CO. KG


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