Last synced on 4 July 2025 at 11:05 pm

RUBELLA IGG ANTIBODY ELISA TEST SYS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K841200
510(k) Type
Traditional
Applicant
ORTHO DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/1984
Days to Decision
61 days

RUBELLA IGG ANTIBODY ELISA TEST SYS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K841200
510(k) Type
Traditional
Applicant
ORTHO DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/1984
Days to Decision
61 days