K-number	K011699
Device name	VACUETTE EVACUATED BLOOD COLLECTION TUBES
Applicant	Greiner Bio-One Vacuette North America
Product code	JKA
Device class	Class II
Decision date	Jun 28, 2001
Decision	Substantially Equivalent
Regulation	862.1675

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View the full FDA submission: accessdata.fda.gov

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VACUETTE EVACUATED BLOOD COLLECTION TUBES

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