K-number	K061832
Device name	JOSTRA HLM TUBING SETS WITH SAFELINE COATING
Applicant	Maquet Cardiopulmonary, AG
Product code	DWF
Device class	Class II
Decision date	Aug 11, 2006
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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JOSTRA HLM TUBING SETS WITH SAFELINE COATING

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