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OKMETER DIRECT BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K132633
510(k) Type
Traditional
Applicant
OK BIOTECH CO., LTD.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
8/14/2014
Days to Decision
357 days
Submission Type
Summary

OKMETER DIRECT BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K132633
510(k) Type
Traditional
Applicant
OK BIOTECH CO., LTD.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
8/14/2014
Days to Decision
357 days
Submission Type
Summary