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ON CALL VIVID BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K123010
510(k) Type
Traditional
Applicant
ACON LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2012
Days to Decision
78 days
Submission Type
Summary

ON CALL VIVID BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K123010
510(k) Type
Traditional
Applicant
ACON LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2012
Days to Decision
78 days
Submission Type
Summary