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FDA 510(k) Applications Submitted by TRUMPF KREUZER MEDIZIN SYSTEME GMBH + CO.KG
FDA 510(k) Number
Submission Date
Device Name
Applicant
K102758
09/23/2010
TRULIGHT 5520 AND TRULIGHT 5320
TRUMPF KREUZER MEDIZIN SYSTEME GMBH + CO.KG
K061317
05/11/2006
ILED
TRUMPF KREUZER MEDIZIN SYSTEME GMBH + CO.KG
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