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VISUWELL(R) REAGIN TEST (MODIFICATION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900338
510(k) Type
Traditional
Applicant
ADI DIAGNOSTICS, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
4/10/1990
Days to Decision
77 days

VISUWELL(R) REAGIN TEST (MODIFICATION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900338
510(k) Type
Traditional
Applicant
ADI DIAGNOSTICS, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
4/10/1990
Days to Decision
77 days