K-number	K882198
Device name	MINIMON 7132B PATIENT MONITOR
Applicant	Kontron Instruments, Inc.
Product code	DPS
Device class	Class II
Decision date	Jul 28, 1988
Decision	Substantially Equivalent
Regulation	870.2340

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View the full FDA submission: accessdata.fda.gov

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MINIMON 7132B PATIENT MONITOR

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