K-number	K010928
Device name	PROLITE VL PULSED LIGHT SYSTEM
Applicant	Medical Bio Care Sweden AB
Product code	GEX
Device class	Class II
Decision date	Jun 19, 2001
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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PROLITE VL PULSED LIGHT SYSTEM

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