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MODIFIED LABSYSTEMS' RUBELLA IGG EIA TEST KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890091
510(k) Type
Traditional
Applicant
LABSYSTEMS, INC.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
2/3/1989
Days to Decision
29 days

MODIFIED LABSYSTEMS' RUBELLA IGG EIA TEST KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890091
510(k) Type
Traditional
Applicant
LABSYSTEMS, INC.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
2/3/1989
Days to Decision
29 days