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VOLUMET CD4 + AND CD8 + T LYMPHOCYTE COUNT TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940003
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/1995
Days to Decision
654 days
Submission Type
Summary

VOLUMET CD4 + AND CD8 + T LYMPHOCYTE COUNT TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940003
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/1995
Days to Decision
654 days
Submission Type
Summary