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ORTHO RUBELLA ELISA TEST SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822342
510(k) Type
Traditional
Applicant
ORTHO DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/1983
Days to Decision
225 days

ORTHO RUBELLA ELISA TEST SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822342
510(k) Type
Traditional
Applicant
ORTHO DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/1983
Days to Decision
225 days