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ULTRA BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K912440
510(k) Type
Traditional
Applicant
HOME DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1991
Days to Decision
44 days
Submission Type
Statement

ULTRA BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K912440
510(k) Type
Traditional
Applicant
HOME DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1991
Days to Decision
44 days
Submission Type
Statement