K-number	K902228
Device name	MODIFIED EPICARDIAL ARRAY
Applicant	C.R. Bard, Inc.
Product code	DRF
Device class	Class II
Decision date	Jul 6, 1990
Decision	Substantially Equivalent
Regulation	870.1220

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View the full FDA submission: accessdata.fda.gov

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MODIFIED EPICARDIAL ARRAY

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