FDA 510(k) Applications Submitted by EB NEURO, S.P.A.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K121996 |
07/09/2012 |
BE PLUS LTM AMPLIFIER GWI AMPLIFIER |
EB NEURO, S.P.A. |
| K073415 |
12/04/2007 |
NEMUS SYSTEM; NEMUS PC PERIPHERAL |
EB NEURO, S.P.A. |
| K142064 |
07/30/2014 |
GALILEO NT |
EB NEURO, S.P.A. |
| K133517 |
11/15/2013 |
NEMUS 2 SYSTEM |
EB NEURO, S.P.A. |
| K041198 |
05/07/2004 |
NIC36 AMPLIFIER |
EB NEURO, S.P.A. |
| K061996 |
07/14/2006 |
SANDMAN POCKET |
EB NEURO, S.P.A. |
| K053606 |
12/27/2005 |
BE PLUS / AURA-LTM64 AMPLIFIER |
EB NEURO, S.P.A. |
| K150220 |
01/30/2015 |
STM 9000 Basic, STM 9000 Standard, STM 9000 Fast, STM 9000 Ultra-Fast |
EB NEURO, S.P.A. |
| K040113 |
01/20/2004 |
SANDMAN SD20 AMPLIFIER |
EB NEURO, S.P.A. |
| K003154 |
10/10/2000 |
MIZAR, BASIS BE, SANDMAN DIGITAL |
EB NEURO, S.P.A. |
| K093728 |
12/03/2009 |
BE MICRO, TREA |
EB NEURO, S.P.A. |
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