K-number	K012059
Device name	8100/8500 VITAL SIGNS MONITOR
Applicant	Criticare Systems, Inc.
Product code	MWI
Device class	Class II
Decision date	Aug 1, 2001
Decision	Substantially Equivalent
Regulation	870.2300

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View the full FDA submission: accessdata.fda.gov

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8100/8500 VITAL SIGNS MONITOR

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