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ACURA PLUS BLOOD GLUCOSE MONITORING SYSTEM; ACURA PLUS BLOOD GLUCOSE METER; ACURA CONTROL SOLUTION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103278
510(k) Type
Special
Applicant
i-SENS, Inc.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
10/28/2011
Days to Decision
357 days
Submission Type
Summary

ACURA PLUS BLOOD GLUCOSE MONITORING SYSTEM; ACURA PLUS BLOOD GLUCOSE METER; ACURA CONTROL SOLUTION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103278
510(k) Type
Special
Applicant
i-SENS, Inc.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
10/28/2011
Days to Decision
357 days
Submission Type
Summary