K-number	K960272
Device name	EAGLE 3000/3100 PATIENT MONITOR
Applicant	Marquette Electronics, Inc.
Product code	MLD
Device class	Class II
Decision date	Oct 2, 1996
Decision	Substantially Equivalent
Regulation	870.1025

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View the full FDA submission: accessdata.fda.gov

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EAGLE 3000/3100 PATIENT MONITOR

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