K-number	K120134
Device name	IPS E.MAX PRESS MULTI
Applicant	Ivoclar Vivadent, AG
Product code	EIH
Device class	Class II
Decision date	Jun 25, 2012
Decision	Substantially Equivalent
Regulation	872.6660

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Source

View the full FDA submission: accessdata.fda.gov

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IPS E.MAX PRESS MULTI

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