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fMRI Hardware System

Page Type
Cleared 510(K)
510(k) Number
K191032
510(k) Type
Traditional
Applicant
Nordicneurolab AS
Country
Norway
FDA Decision
Substantially Equivalent
Decision Date
11/27/2019
Days to Decision
223 days
Submission Type
Summary

fMRI Hardware System

Page Type
Cleared 510(K)
510(k) Number
K191032
510(k) Type
Traditional
Applicant
Nordicneurolab AS
Country
Norway
FDA Decision
Substantially Equivalent
Decision Date
11/27/2019
Days to Decision
223 days
Submission Type
Summary