Last synced on 30 May 2025 at 11:05 pm

VEGA RETIC AUTOMATED HEMATOLOGY ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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