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FMRI HARDWARE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080515
510(k) Type
Traditional
Applicant
NORDICNEUROLAB
Country
Norway
FDA Decision
Substantially Equivalent
Decision Date
5/16/2008
Days to Decision
81 days
Submission Type
Summary