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MODIFICATION TO INTEGRA REAGENT CASSETTE FOR HEMOGLOBIN A1C

Page Type
Cleared 510(K)
510(k) Number
K003120
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2000
Days to Decision
74 days
Submission Type
Summary

MODIFICATION TO INTEGRA REAGENT CASSETTE FOR HEMOGLOBIN A1C

Page Type
Cleared 510(K)
510(k) Number
K003120
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2000
Days to Decision
74 days
Submission Type
Summary