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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