K-number	K953859
Device name	BOND-IT DUAL CURE ACTIVATOR
Applicant	Jeneric/Pentron, Inc.
Product code	KLE
Device class	Class II
Decision date	Sep 7, 1995
Decision	Substantially Equivalent
Regulation	872.3200

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View the full FDA submission: accessdata.fda.gov

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BOND-IT DUAL CURE ACTIVATOR

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