K-number	K850619
Device name	BEDSIDE PATIENT MONITOR W/MODULES
Applicant	Midwest Analog & Digital, Inc.
Product code	DRT
Device class	Class II
Decision date	Jun 6, 1985
Decision	Substantially Equivalent
Regulation	870.2300

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View the full FDA submission: accessdata.fda.gov

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BEDSIDE PATIENT MONITOR W/MODULES

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