K-number	K032252
Device name	MODEL 120 SERIES MATERNAL/FETAL MONITOR
Applicant	Ge Medical Systems Information Technologies
Product code	HGM
Device class	Class II
Decision date	Aug 21, 2003
Decision	Substantially Equivalent
Regulation	884.2740

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View the full FDA submission: accessdata.fda.gov

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MODEL 120 SERIES MATERNAL/FETAL MONITOR

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