K-number	K093431
Device name	CLEARWAY OTW MODEL 85912
Applicant	Atrium Medical Corp.
Product code	DQY
Device class	Class II
Decision date	Apr 20, 2010
Decision	Substantially Equivalent
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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CLEARWAY OTW MODEL 85912

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