K-number	K991783
Device name	AB-180 XC SYSTEM, MODEL AB-180XC
Applicant	Cardiacassist, Inc.
Product code	KFM
Device class	Class II
Decision date	Nov 1, 2000
Decision	Substantially Equivalent
Regulation	870.4360

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View the full FDA submission: accessdata.fda.gov

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AB-180 XC SYSTEM, MODEL AB-180XC

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