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MODIFICATION TO ACCU-CHEK ACTIVE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K021448
510(k) Type
Special
Applicant
ROCHE DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2002
Days to Decision
28 days
Submission Type
Summary

MODIFICATION TO ACCU-CHEK ACTIVE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K021448
510(k) Type
Special
Applicant
ROCHE DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2002
Days to Decision
28 days
Submission Type
Summary