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DYNAMIC NEUROSCREENING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K141208
510(k) Type
Traditional
Applicant
Prosenex
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2014
Days to Decision
75 days
Submission Type
Summary

DYNAMIC NEUROSCREENING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K141208
510(k) Type
Traditional
Applicant
Prosenex
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2014
Days to Decision
75 days
Submission Type
Summary