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FDA 510(k), K091393, ELEKTA NEUROMAG WITH MAXFILTER
FDA 510(k), K091393, ELEKTA NEUROMAG WITH MAXFILTER
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510(K) Number: K091393
Device Name: ELEKTA NEUROMAG WITH MAXFILTER
Manufacturer: ELEKTA NEUROMAG OY
Device Classification Name: Source Localization Software For Electroencephalograph Or Magnetoencephalograph
Regulation Number: 882.1400
Classification Product Code: OLX
Date Received: 05/11/2009
Decision Date: 10/26/2010
Regulation Medical Specialty: Neurology
Device Name: ELEKTA NEUROMAG WITH MAXFILTER
Manufacturer: ELEKTA NEUROMAG OY
Device Classification Name: Source Localization Software For Electroencephalograph Or Magnetoencephalograph
Regulation Number: 882.1400
Classification Product Code: OLX
Date Received: 05/11/2009
Decision Date: 10/26/2010
Regulation Medical Specialty: Neurology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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