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BIOTEST ANTI-EBV RECOMBINANT, EA IGM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983842
510(k) Type
Traditional
Applicant
Biotest Diagnostics Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/1999
Days to Decision
222 days
Submission Type
Summary

BIOTEST ANTI-EBV RECOMBINANT, EA IGM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983842
510(k) Type
Traditional
Applicant
Biotest Diagnostics Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/1999
Days to Decision
222 days
Submission Type
Summary