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PRESTIGE BLOOD GLUCOSE MONITORING SYSTEM,METER,TEST STRIPS & PRESTIGE HIGH AND LOW GLUCOSE CONTROL

Page Type
Cleared 510(K)
510(k) Number
K960855
510(k) Type
Traditional
Applicant
HOME DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/1996
Days to Decision
251 days
Submission Type
Statement

PRESTIGE BLOOD GLUCOSE MONITORING SYSTEM,METER,TEST STRIPS & PRESTIGE HIGH AND LOW GLUCOSE CONTROL

Page Type
Cleared 510(K)
510(k) Number
K960855
510(k) Type
Traditional
Applicant
HOME DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/1996
Days to Decision
251 days
Submission Type
Statement