K-number	K890817
Device name	OMNI-TRAK (PATIENT MONITOR)
Applicant	Invivo Research, Inc.
Product code	CCK
Device class	Class II
Decision date	Aug 10, 1989
Decision	Substantially Equivalent
Regulation	868.1400

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Source

View the full FDA submission: accessdata.fda.gov

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OMNI-TRAK (PATIENT MONITOR)

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