K-number	K003442
Device name	MODIFICATION TO EDI VERIS SYSTEM
Applicant	Electro-Diagnostic Imaging, Inc.
Product code	HLX
Device class	Class II
Decision date	May 4, 2001
Decision	Substantially Equivalent
Regulation	886.1630

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO EDI VERIS SYSTEM

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