K-number	K896819
Device name	VAMP VENOUS/ARTERIAL BLOOD MANAGEMENT PROTECTION
Applicant	Baxter Healthcare Corp
Product code	KRA
Device class	Class II
Decision date	Jan 19, 1990
Decision	Substantially Equivalent
Regulation	870.1210

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View the full FDA submission: accessdata.fda.gov

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VAMP VENOUS/ARTERIAL BLOOD MANAGEMENT PROTECTION

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