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ELEKTA NEUROMAG WITH MAXFILTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091393
510(k) Type
Traditional
Applicant
ELEKTA NEUROMAG OY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2010
Days to Decision
533 days
Submission Type
Summary

ELEKTA NEUROMAG WITH MAXFILTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091393
510(k) Type
Traditional
Applicant
ELEKTA NEUROMAG OY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2010
Days to Decision
533 days
Submission Type
Summary