K-number	K933830
Device name	KONICA LD-4500 LASER DIGITIZER
Applicant	Konica Medical Corp.
Product code	LMA
Device class	Class II
Decision date	Dec 14, 1993
Decision	Substantially Equivalent
Regulation	892.2030

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View the full FDA submission: accessdata.fda.gov

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KONICA LD-4500 LASER DIGITIZER

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