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NOVA MAX PLUS BLOOD GLUCOSE AND B-KETONE MONITOR SYSTEM, NOVA MAX PLUS B-KETONE CONTROL SOLUTIONS, NOVA MAX BLOOD GLUCOS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091547
510(k) Type
Traditional
Applicant
NOVA BIOMEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/2010
Days to Decision
233 days
Submission Type
Summary

NOVA MAX PLUS BLOOD GLUCOSE AND B-KETONE MONITOR SYSTEM, NOVA MAX PLUS B-KETONE CONTROL SOLUTIONS, NOVA MAX BLOOD GLUCOS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091547
510(k) Type
Traditional
Applicant
NOVA BIOMEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/2010
Days to Decision
233 days
Submission Type
Summary