K-number	K883109
Device name	MINIMON 7136B PATIENT MONITOR
Applicant	Kontron, Inc.
Product code	DRT
Device class	Class II
Decision date	Jan 17, 1989
Decision	Substantially Equivalent
Regulation	870.2300

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View the full FDA submission: accessdata.fda.gov

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MINIMON 7136B PATIENT MONITOR

Everything you need for a 510(k) submission. Nothing you don't.