K-number	K092117
Device name	SCENAR, MODEL 10
Applicant	Ritm Okb Zao
Product code	GZJ
Device class	Class II
Decision date	May 28, 2010
Decision	Substantially Equivalent
Regulation	882.5890

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Source

View the full FDA submission: accessdata.fda.gov

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SCENAR, MODEL 10

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