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ZYMMUNE(TM) CD4/CD8 CELL MONITORING KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933878
510(k) Type
Traditional
Applicant
INTRACEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1995
Days to Decision
827 days
Submission Type
Summary

ZYMMUNE(TM) CD4/CD8 CELL MONITORING KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933878
510(k) Type
Traditional
Applicant
INTRACEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1995
Days to Decision
827 days
Submission Type
Summary