K-number	K080734
Device name	FLOWSCREEN, FLOWSCREEN/CORSCREEN, FLOWSCREEN CT
Applicant	Viasys Healthcare GmbH
Product code	BTY
Device class	Class II
Decision date	Jun 26, 2008
Decision	Substantially Equivalent
Regulation	868.1890

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View the full FDA submission: accessdata.fda.gov

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FLOWSCREEN, FLOWSCREEN/CORSCREEN, FLOWSCREEN CT

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