K-number	K053025
Device name	JOSTRA HLM TUBING SET
Applicant	Maquet Cardiopulmonary, AG
Product code	DWE
Device class	Class II
Decision date	Nov 10, 2005
Decision	Substantially Equivalent
Regulation	870.4390

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View the full FDA submission: accessdata.fda.gov

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JOSTRA HLM TUBING SET

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