K-number	K033933
Device name	POWERLITE 600 EX SYSTEM
Applicant	Preswede AB
Product code	GEX
Device class	Class II
Decision date	Mar 16, 2004
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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POWERLITE 600 EX SYSTEM

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