K-number	K072323
Device name	MASTERSCREEN & OXYCON CPX
Applicant	Viasys Healthcare GmbH
Product code	BZC
Device class	Class II
Decision date	Oct 10, 2007
Decision	Substantially Equivalent
Regulation	868.1880

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View the full FDA submission: accessdata.fda.gov

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MASTERSCREEN & OXYCON CPX

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