K-number	K012915
Device name	DINAMAP PRO 1000 MONITOR, MODEL 1000
Applicant	Ge Medical Systems Information Technologies
Product code	MHX
Device class	Class II
Decision date	Mar 21, 2002
Decision	Substantially Equivalent
Regulation	870.1025

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View the full FDA submission: accessdata.fda.gov

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DINAMAP PRO 1000 MONITOR, MODEL 1000

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