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FDA 510(k) Applications Submitted by THE MAGSTIM COMPANY LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K051864
07/08/2005
MAGSTIM RAPID2, MAGSTIM SUPER RAPID2, MODELS 3004-000, 3005-00
THE MAGSTIM COMPANY LTD.
K080499
02/25/2008
MAGSTIM DOUBLE 70MM AIR FILM COIL, MODEL 3910-00
THE MAGSTIM COMPANY LTD.
K071349
05/14/2007
NEUROSIGN LARYNGEAL ELECTRODES
THE MAGSTIM COMPANY LTD.
K083242
11/03/2008
NEUROSIGN AVALANCHE MOTOR NERVE MONITOR
THE MAGSTIM COMPANY LTD.
K964869
12/04/1996
NEUROSIGN 800, 8 CHANNEL MOTOR NERVE MONITOR
THE MAGSTIM COMPANY LTD.
K980148
01/15/1998
NEUROSIGN 800, 8 CHANNEL MOTOR NERVE MONITOR
THE MAGSTIM COMPANY LTD.
K053141
11/09/2005
NEUROSIGN MOTOR NERVE MONITOR, MODELS NEUROSIGN 400 & 800
THE MAGSTIM COMPANY LTD.
K130403
02/19/2013
MAGSTIM DOUBLE 70-2 COIL
THE MAGSTIM COMPANY LTD.
K991583
05/07/1999
NEUROSIGN 400, 4 CHANNEL MOTOR NERVE MONITOR
THE MAGSTIM COMPANY LTD.
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