K-number	K082071
Device name	ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT
Applicant	Adpharma, Inc.
Product code	LBH
Device class	Class II
Decision date	Oct 2, 2008
Decision	Substantially Equivalent
Regulation	872.3260

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View the full FDA submission: accessdata.fda.gov

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ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT

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