K-number	K132750
Device name	ILLUMINA MISEQDX CYSTIC FIBROSIS CLINICAL SEQUENCING ASSAY
Applicant	Illumina, Inc.
Product code	PFS
Device class	Class II
Decision date	Nov 19, 2013
Decision	Substantially Equivalent
Regulation	866.5900

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View the full FDA submission: accessdata.fda.gov

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ILLUMINA MISEQDX CYSTIC FIBROSIS CLINICAL SEQUENCING ASSAY

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