K-number	K102758
Device name	TRULIGHT 5520 AND TRULIGHT 5320
Applicant	Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg
Product code	FSY
Device class	Class II
Decision date	Oct 26, 2010
Decision	Substantially Equivalent
Regulation	878.4580

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Source

View the full FDA submission: accessdata.fda.gov

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TRULIGHT 5520 AND TRULIGHT 5320

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