K-number	K072976
Device name	MODEL 250CX SERIES MATERNAL/FETAL MONITOR
Applicant	GE Healthcare
Product code	HGM
Device class	Class II
Decision date	Dec 20, 2007
Decision	Substantially Equivalent
Regulation	884.2740

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Source

View the full FDA submission: accessdata.fda.gov

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MODEL 250CX SERIES MATERNAL/FETAL MONITOR

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