K-number	K123556
Device name	MORTARA SURVEYOR PATIENT MONITOR
Applicant	Mortara Instrument, Inc.
Product code	MHX
Device class	Class II
Decision date	Mar 22, 2013
Decision	Substantially Equivalent
Regulation	870.1025

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Source

View the full FDA submission: accessdata.fda.gov

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MORTARA SURVEYOR PATIENT MONITOR

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