K-number	K071610
Device name	MEDIAID PULSE OXIMETER M30 AND M34
Applicant	Mediaid, Inc.
Product code	DQA
Device class	Class II
Decision date	Nov 5, 2007
Decision	Substantially Equivalent
Regulation	870.2700

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View the full FDA submission: accessdata.fda.gov

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MEDIAID PULSE OXIMETER M30 AND M34

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