K-number	K946050
Device name	LIQUISPEX(TM) LIQUID CRP CONTROL LEVEL 1 AND 2
Applicant	Clinical Controls, Inc.
Product code	DCK
Device class	Class II
Decision date	Feb 10, 1995
Decision	Substantially Equivalent
Regulation	866.5270

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View the full FDA submission: accessdata.fda.gov

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LIQUISPEX(TM) LIQUID CRP CONTROL LEVEL 1 AND 2

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