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MODIFICATION TO FMRI HARDWARE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092253
510(k) Type
Special
Applicant
NORDICNEUROLAB
Country
Norway
FDA Decision
Substantially Equivalent
Decision Date
10/8/2009
Days to Decision
72 days
Submission Type
Summary