K-number	K910610
Device name	INTERPLAK HOME PLAQUE REMOVAL INSTRUMENT
Applicant	Bausch & Lomb, Inc.
Product code	JEQ
Device class	Class I
Decision date	Jul 9, 1991
Decision	Substantially Equivalent
Regulation	872.6865

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View the full FDA submission: accessdata.fda.gov

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INTERPLAK HOME PLAQUE REMOVAL INSTRUMENT

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