K-number	K913995
Device name	VITALERT 3000 MONITORING SYSTEM
Applicant	Draeger Medical, Inc.
Product code	CCK
Device class	Class II
Decision date	Nov 3, 1992
Decision	Substantially Equivalent
Regulation	868.1400

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View the full FDA submission: accessdata.fda.gov

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VITALERT 3000 MONITORING SYSTEM

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