K-number	K021154
Device name	GOLDWAY PATIENT MONITOR, MODEL # UT4000F
Applicant	Goldway Us, Inc.
Product code	MWI
Device class	Class II
Decision date	Apr 11, 2003
Decision	Substantially Equivalent
Regulation	870.2300

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View the full FDA submission: accessdata.fda.gov

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GOLDWAY PATIENT MONITOR, MODEL # UT4000F

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