K-number	K161928
Device name	CAPI 3 IMMUNOTYPING, CAPILLARYS 3 TERA, IT/IF CONTROL
Applicant	Sebia
Product code	CFF
Device class	Class II
Decision date	Dec 21, 2016
Decision	Substantially Equivalent
Regulation	866.5510

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View the full FDA submission: accessdata.fda.gov

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CAPI 3 IMMUNOTYPING, CAPILLARYS 3 TERA, IT/IF CONTROL

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