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Elekta Neuromag OY
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K091393
ELEKTA NEUROMAG WITH MAXFILTER
October 26, 2010
K081430
ELEKTA NEUROMAG WITH MAXWELL FILTER WITH INTERNAL ACTIVE SHIELDING
July 28, 2008
K050035
ELEKTA NEUROMAG WITH MAXWELL FILTER
January 25, 2005
K041264
ELEKTA OY
August 10, 2004