K-number	K061317
Device name	ILED
Applicant	Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg
Product code	FSY
Device class	Class II
Decision date	Jun 22, 2006
Decision	Substantially Equivalent
Regulation	878.4580

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Source

View the full FDA submission: accessdata.fda.gov

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ILED

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