K-number	K013878
Device name	CYBERMED, INC., V-WORKS
Applicant	Cybermed, Inc.
Product code	LLZ
Device class	Class II
Decision date	Dec 7, 2001
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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CYBERMED, INC., V-WORKS

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