K-number	K080592
Device name	HLM TUBING SET WITH BIOLINE COATING
Applicant	Maquet Cardiopulmonary, AG
Product code	DWE
Device class	Class II
Decision date	Sep 11, 2008
Decision	Substantially Equivalent
Regulation	870.4390

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View the full FDA submission: accessdata.fda.gov

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HLM TUBING SET WITH BIOLINE COATING

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