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MODIFICATION TO HYPOGUARD ADVANCE BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K031388
510(k) Type
Special
Applicant
HYPOGUARD USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2003
Days to Decision
20 days
Submission Type
Summary

MODIFICATION TO HYPOGUARD ADVANCE BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K031388
510(k) Type
Special
Applicant
HYPOGUARD USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2003
Days to Decision
20 days
Submission Type
Summary