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FOCUS BLOOD GLUCOSE MONITORING SYSTEM, FOCUS PRO 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
K131013
510(k) Type
Traditional
Applicant
NOVA BIOMEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2013
Days to Decision
189 days
Submission Type
Summary

FOCUS BLOOD GLUCOSE MONITORING SYSTEM, FOCUS PRO 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
K131013
510(k) Type
Traditional
Applicant
NOVA BIOMEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2013
Days to Decision
189 days
Submission Type
Summary