K-number	K030279
Device name	REPROCESSED ELECTROPHYSIOLOGY CATHETER
Applicant	Alliance Medical Corp.
Product code	NLH
Device class	Class II
Decision date	Oct 3, 2003
Decision	Substantially Equivalent
Regulation	870.1220

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View the full FDA submission: accessdata.fda.gov

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REPROCESSED ELECTROPHYSIOLOGY CATHETER

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