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VEGA RETIC AUTOMATED HEMATOLOGY ANALYZER

Page Type
Cleared 510(K)
510(k) Number
K990311
510(k) Type
Traditional
Applicant
ABX DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1999
Days to Decision
58 days
Submission Type
Summary

VEGA RETIC AUTOMATED HEMATOLOGY ANALYZER

Page Type
Cleared 510(K)
510(k) Number
K990311
510(k) Type
Traditional
Applicant
ABX DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1999
Days to Decision
58 days
Submission Type
Summary