K-number	K974655
Device name	PREPTECH(TM) 200 CAVITY PREPARATION SYSTEM
Applicant	Prep Technology Corp.
Product code	KOJ
Device class	Class II
Decision date	Jul 9, 1998
Decision	Substantially Equivalent
Regulation	872.6080

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View the full FDA submission: accessdata.fda.gov

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PREPTECH(TM) 200 CAVITY PREPARATION SYSTEM

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