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FERRITIN GENERATION 2

Page Type
Cleared 510(K)
510(k) Number
K031650
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2003
Days to Decision
50 days
Submission Type
Summary

FERRITIN GENERATION 2

Page Type
Cleared 510(K)
510(k) Number
K031650
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2003
Days to Decision
50 days
Submission Type
Summary