K-number	K082887
Device name	PM-1000F+PATIENT MONITOR
Applicant	Advanced Instrumentations, Inc.
Product code	MWI
Device class	Class II
Decision date	Jan 16, 2009
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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PM-1000F+PATIENT MONITOR

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