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SENSOREX BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K980573
510(k) Type
Traditional
Applicant
CHRONIMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1998
Days to Decision
163 days
Submission Type
Statement

SENSOREX BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K980573
510(k) Type
Traditional
Applicant
CHRONIMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1998
Days to Decision
163 days
Submission Type
Statement