K-number	K113390
Device name	LASER INDIRECT OPHTHALMOSCOPE 500(LIO-500)
Applicant	Meridian AG
Product code	GEX
Device class	Class II
Decision date	Feb 14, 2012
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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LASER INDIRECT OPHTHALMOSCOPE 500(LIO-500)

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