K-number	K943664
Device name	INTERMATE XLV ELASTOMERIC INFUSION SYSTEM
Applicant	Baxter Healthcare Corp
Product code	MEB
Device class	Class II
Decision date	Nov 3, 1994
Decision	Substantially Equivalent
Regulation	880.5725

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View the full FDA submission: accessdata.fda.gov

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INTERMATE XLV ELASTOMERIC INFUSION SYSTEM

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