K-number	K012440
Device name	MODIFICATION TO CLEARFIL LINER BOND 2V
Applicant	Kuraray Medical, Inc.
Product code	KLE
Device class	Class II
Decision date	Sep 5, 2001
Decision	Substantially Equivalent
Regulation	872.3200

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO CLEARFIL LINER BOND 2V

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