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PRESTIGE LX BLOOD GLUCOSE TEST SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K992988
510(k) Type
Special
Applicant
HOME DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/24/1999
Days to Decision
21 days
Submission Type
Statement

PRESTIGE LX BLOOD GLUCOSE TEST SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K992988
510(k) Type
Special
Applicant
HOME DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/24/1999
Days to Decision
21 days
Submission Type
Statement