K-number	K131513
Device name	SCENAR (SCELAP, ENISAR, IPENS) CUTANEOUS ELECTRODE FAMILY
Applicant	Ritm Okb Zao
Product code	GZJ
Device class	Class II
Decision date	Jul 11, 2014
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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SCENAR (SCELAP, ENISAR, IPENS) CUTANEOUS ELECTRODE FAMILY

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