K-number	K191456
Device name	Campylobacter Quik Chek
Applicant	Techlab, Inc.
Product code	LQP
Device class	Class I
Decision date	Jun 20, 2019
Decision	Substantially Equivalent
Regulation	866.3110

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Source

View the full FDA submission: accessdata.fda.gov

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Campylobacter Quik Chek

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