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EBV/EA-CHECK TM TEST KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903612
510(k) Type
Traditional
Applicant
DIAGNOSTIC TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1990
Days to Decision
68 days

EBV/EA-CHECK TM TEST KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903612
510(k) Type
Traditional
Applicant
DIAGNOSTIC TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1990
Days to Decision
68 days