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SURESET INFUSION SET, MODEL 8023

Page Type
Cleared 510(K)
510(k) Number
K012429
510(k) Type
Traditional
Applicant
APPLIED DIABETES RESEARCH, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/2001
Days to Decision
98 days
Submission Type
Summary

SURESET INFUSION SET, MODEL 8023

Page Type
Cleared 510(K)
510(k) Number
K012429
510(k) Type
Traditional
Applicant
APPLIED DIABETES RESEARCH, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/2001
Days to Decision
98 days
Submission Type
Summary