K-number	K903849
Device name	MODEL RD-1200 RUBY LASER SYSTEM
Applicant	Charles L. Rose and Co., Inc.
Product code	GEX
Device class	Class II
Decision date	Sep 5, 1990
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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MODEL RD-1200 RUBY LASER SYSTEM

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