K-number	K130076
Device name	PROMOLUX, PROMOLUX HI, WEROPRESS, PREMECO PCS
Applicant	Merz Dental GmbH
Product code	EBI
Device class	Class II
Decision date	Aug 22, 2013
Decision	Substantially Equivalent
Regulation	872.3760

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View the full FDA submission: accessdata.fda.gov

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PROMOLUX, PROMOLUX HI, WEROPRESS, PREMECO PCS

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