K-number	K042130
Device name	AURA CPAP PATIENT INTERFACE
Applicant	Aeiomed, Inc.
Product code	BZD
Device class	Class II
Decision date	Sep 8, 2004
Decision	Substantially Equivalent
Regulation	868.5905

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View the full FDA submission: accessdata.fda.gov

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AURA CPAP PATIENT INTERFACE

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