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FDA 510(k) Applications Submitted by ELEKTA NEUROMAG OY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K041264
05/12/2004
ELEKTA OY
ELEKTA NEUROMAG OY
K091393
05/11/2009
ELEKTA NEUROMAG WITH MAXFILTER
ELEKTA NEUROMAG OY
K081430
05/21/2008
ELEKTA NEUROMAG WITH MAXWELL FILTER WITH INTERNAL ACTIVE SHIELDING
ELEKTA NEUROMAG OY
K050035
01/07/2005
ELEKTA NEUROMAG WITH MAXWELL FILTER
ELEKTA NEUROMAG OY
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