K-number	K994182
Device name	PULPDENT CAVITY PREPARATION 1, PULPDENT CAVITY PREPARATION 1 WITH FLUORIDE
Applicant	Pulpdent Corp.
Product code	LBH
Device class	Class II
Decision date	Feb 23, 2000
Decision	Substantially Equivalent
Regulation	872.3260

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View the full FDA submission: accessdata.fda.gov

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PULPDENT CAVITY PREPARATION 1, PULPDENT CAVITY PREPARATION 1 WITH FLUORIDE

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