K-number	K000192
Device name	E3 MICROPROB SERIES OF LASERS AND ACCESSORIES
Applicant	Martin Uram, MD
Product code	GEX
Device class	Class II
Decision date	Apr 10, 2000
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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E3 MICROPROB SERIES OF LASERS AND ACCESSORIES

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