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INTEGRA(TM) BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K893404
510(k) Type
Traditional
Applicant
APPRISE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1989
Days to Decision
93 days

INTEGRA(TM) BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K893404
510(k) Type
Traditional
Applicant
APPRISE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1989
Days to Decision
93 days