K-number	K942180
Device name	KEELER MULTILASE 3000
Applicant	Keeler Instruments, Inc.
Product code	HQF
Device class	Class II
Decision date	Nov 22, 1994
Decision	Substantially Equivalent
Regulation	886.4390

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View the full FDA submission: accessdata.fda.gov

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KEELER MULTILASE 3000

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