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SURESTEP BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K984261
510(k) Type
Traditional
Applicant
LIFESCAN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/1999
Days to Decision
175 days
Submission Type
Summary

SURESTEP BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K984261
510(k) Type
Traditional
Applicant
LIFESCAN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/1999
Days to Decision
175 days
Submission Type
Summary