K-number	K090533
Device name	HLM TUBING SET WITH SOFTLINE COATING
Applicant	Maquet Cardiopulmonary, AG
Product code	DWF
Device class	Class II
Decision date	Dec 18, 2009
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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HLM TUBING SET WITH SOFTLINE COATING

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