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LIQUIDCHEK DIABETES CONTROL; LEVEL 1, LEVEL 2, LEVEL 3, TRILEVEL MINIPAK

Page Type
Cleared 510(K)
510(k) Number
K123798
510(k) Type
Traditional
Applicant
Bio-Rad Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2013
Days to Decision
30 days
Submission Type
Summary

LIQUIDCHEK DIABETES CONTROL; LEVEL 1, LEVEL 2, LEVEL 3, TRILEVEL MINIPAK

Page Type
Cleared 510(K)
510(k) Number
K123798
510(k) Type
Traditional
Applicant
Bio-Rad Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2013
Days to Decision
30 days
Submission Type
Summary