K-number	K820179
Device name	ERIKA CAPD PREP KIT #30-9501-5
Applicant	Erika, Inc.
Product code	FKX
Device class	Class II
Decision date	Feb 19, 1982
Decision	Substantially Equivalent
Regulation	876.5630

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View the full FDA submission: accessdata.fda.gov

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ERIKA CAPD PREP KIT #30-9501-5

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