K-number	K963576
Device name	MOBILE MEDICAL MONITOR (M3(A))
Applicant	Scientific Applications
Product code	DRT
Device class	Class II
Decision date	Feb 28, 1997
Decision	Substantially Equivalent
Regulation	870.2300

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View the full FDA submission: accessdata.fda.gov

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MOBILE MEDICAL MONITOR (M3(A))

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