K-number	K780732
Device name	PROCAINAMIDE CALIBRATOR KIT
Applicant	Vitek Systems, Inc.
Product code	DLJ
Device class	Class II
Decision date	Nov 22, 1978
Decision	Substantially Equivalent
Regulation	862.3200

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View the full FDA submission: accessdata.fda.gov

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PROCAINAMIDE CALIBRATOR KIT

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