K-number	K022378
Device name	PLASMALITE PULSED LIGHT SYSTEM
Applicant	Medical Bio Care Sweden AB
Product code	GEX
Device class	Class II
Decision date	Oct 18, 2002
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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PLASMALITE PULSED LIGHT SYSTEM

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