K-number	K990311
Device name	VEGA RETIC AUTOMATED HEMATOLOGY ANALYZER
Applicant	Abx Diagnostics
Product code	GKZ
Device class	Class II
Decision date	Mar 31, 1999
Decision	Substantially Equivalent
Regulation	864.5220

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View the full FDA submission: accessdata.fda.gov

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VEGA RETIC AUTOMATED HEMATOLOGY ANALYZER

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