Last synced on 30 May 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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