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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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