K-number	K921381
Device name	MEDGRAPHIX INTL VR 1000 SERIES
Applicant	Medgraphix Intl.
Product code	LMC
Device class	Class II
Decision date	Nov 2, 1992
Decision	Substantially Equivalent
Regulation	892.2040

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Source

View the full FDA submission: accessdata.fda.gov

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MEDGRAPHIX INTL VR 1000 SERIES

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