K-number	K062959
Device name	DMS 300-2, 300-3 AND 300-4
Applicant	Diagnostic Monitoring Software
Product code	MWJ
Device class	Class II
Decision date	Oct 16, 2006
Decision	Substantially Equivalent
Regulation	870.2800

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Source

View the full FDA submission: accessdata.fda.gov

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DMS 300-2, 300-3 AND 300-4

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