K-number	K896417
Device name	KONTRON KOLORMON 7250 PATIENT MONITOR
Applicant	Kontron Instruments, Inc.
Product code	DPS
Device class	Class II
Decision date	Dec 12, 1989
Decision	Substantially Equivalent
Regulation	870.2340

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View the full FDA submission: accessdata.fda.gov

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KONTRON KOLORMON 7250 PATIENT MONITOR

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