K-number	K020253
Device name	4 ALL (DW286A)
Applicant	Ivoclar Vivadent, Inc.
Product code	EJH
Device class	Class II
Decision date	Apr 17, 2002
Decision	Substantially Equivalent
Regulation	872.3710

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View the full FDA submission: accessdata.fda.gov

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4 ALL (DW286A)

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