K-number	K780834
Device name	PREVI DENT PROPHYLAXIS MINT NDC
Applicant	Hoyt Laboratories
Product code	EJR
Device class	Class I
Decision date	Jun 2, 1978
Decision	Substantially Equivalent
Regulation	872.6030

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View the full FDA submission: accessdata.fda.gov

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PREVI DENT PROPHYLAXIS MINT NDC

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