K-number	K962099
Device name	CEDIA PROCAINAMIDE ASSAY
Applicant	Boehringer Mannheim Corp.
Product code	LAR
Device class	Class II
Decision date	Aug 27, 1996
Decision	Substantially Equivalent
Regulation	862.3320

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View the full FDA submission: accessdata.fda.gov

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CEDIA PROCAINAMIDE ASSAY

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