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IDENTEVENT, VERSION 1.0G

Page Type
Cleared 510(K)
510(k) Number
K092039
510(k) Type
Traditional
Applicant
OPTIMA NEUROSCIENCE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2009
Days to Decision
102 days
Submission Type
Summary

IDENTEVENT, VERSION 1.0G

Page Type
Cleared 510(K)
510(k) Number
K092039
510(k) Type
Traditional
Applicant
OPTIMA NEUROSCIENCE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2009
Days to Decision
102 days
Submission Type
Summary