K-number	K912256
Device name	PRECISE(R) BETA QUARTZ GLASS-CERAMIC INSERT
Applicant	Lee Pharmaceuticals
Product code	KLE
Device class	Class II
Decision date	Jul 24, 1991
Decision	Substantially Equivalent
Regulation	872.3200

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View the full FDA submission: accessdata.fda.gov

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PRECISE(R) BETA QUARTZ GLASS-CERAMIC INSERT

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