Last synced on 25 January 2026 at 3:41 am

CEDIA RED BLOOD CELL FOLATE REAGENT PACK, CEDIA FOLATE ASSAY AND ELECSYS FOLATE ASSAY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981931
510(k) Type
Traditional
Applicant
Roche Diagnostics/Boehringer Mannheim GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1998
Days to Decision
84 days
Submission Type
Summary

CEDIA RED BLOOD CELL FOLATE REAGENT PACK, CEDIA FOLATE ASSAY AND ELECSYS FOLATE ASSAY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981931
510(k) Type
Traditional
Applicant
Roche Diagnostics/Boehringer Mannheim GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1998
Days to Decision
84 days
Submission Type
Summary