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OKMETER DIRECT BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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