K-number	K061405
Device name	APNEALINK, MODEL 22302
Applicant	Resmed Germany, Inc.
Product code	MNR
Device class	Class II
Decision date	Jul 25, 2006
Decision	Substantially Equivalent
Regulation	868.2375

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View the full FDA submission: accessdata.fda.gov

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APNEALINK, MODEL 22302

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