K-number	K133265
Device name	QUADROX-IR ADULT AND SMALL ADULT
Applicant	Maquet Cardiopulmonary, AG
Product code	KFM
Device class	Class II
Decision date	Nov 12, 2013
Decision	Substantially Equivalent
Regulation	870.4360

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Source

View the full FDA submission: accessdata.fda.gov

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QUADROX-IR ADULT AND SMALL ADULT

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