K-number	K001763
Device name	CRIT-LINE MONITOR III (CLM III)
Applicant	In-Line Diagnostics Corp.
Product code	MQS
Device class	Class II
Decision date	Dec 20, 2000
Decision	Substantially Equivalent
Regulation	876.5820

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View the full FDA submission: accessdata.fda.gov

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CRIT-LINE MONITOR III (CLM III)

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