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IMMULITE RUBELLA QUANTITATIVE IGG, CATALOG # LKRBQ1 (100 TESTS), LKRBQ5 (500 TESTS)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982078
510(k) Type
Traditional
Applicant
Diagnostic Products Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/1998
Days to Decision
179 days
Submission Type
Summary

IMMULITE RUBELLA QUANTITATIVE IGG, CATALOG # LKRBQ1 (100 TESTS), LKRBQ5 (500 TESTS)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982078
510(k) Type
Traditional
Applicant
Diagnostic Products Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/1998
Days to Decision
179 days
Submission Type
Summary