K-number	K974755
Device name	DYNA VUE 3-D IMAGING PRODUCT
Applicant	Imd Systems, Inc.
Product code	LLZ
Device class	Class II
Decision date	Mar 4, 1998
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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DYNA VUE 3-D IMAGING PRODUCT

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