K-number	K896661
Device name	KEN'S PROPHY GEL - REGULAR
Applicant	Pulpdent Corp.
Product code	EJR
Device class	Class I
Decision date	Feb 14, 1990
Decision	Substantially Equivalent
Regulation	872.6030

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View the full FDA submission: accessdata.fda.gov

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KEN'S PROPHY GEL - REGULAR

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