K-number	K991878
Device name	LUMA-CATH STEERABLE EP CATHETERS
Applicant	Irvine Biomedical, Inc.
Product code	DRF
Device class	Class II
Decision date	Dec 10, 1999
Decision	Substantially Equivalent
Regulation	870.1220

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View the full FDA submission: accessdata.fda.gov

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LUMA-CATH STEERABLE EP CATHETERS

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