K-number	K022084
Device name	ATLAS MONITOR, MODELS 200,210,220
Applicant	Welch Allyn, Inc.
Product code	DQA
Device class	Class II
Decision date	Sep 26, 2002
Decision	Substantially Equivalent
Regulation	870.2700

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View the full FDA submission: accessdata.fda.gov

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ATLAS MONITOR, MODELS 200,210,220

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