K-number	K013634
Device name	BIOTEQUE 3 IN 1 HEMODIALYSIS BLOOD TUBING PACK
Applicant	Bioteque Corp.
Product code	FJK
Device class	Class II
Decision date	Jul 9, 2002
Decision	Unknown
Regulation	876.5820

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View the full FDA submission: accessdata.fda.gov

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BIOTEQUE 3 IN 1 HEMODIALYSIS BLOOD TUBING PACK

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