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FDA 510(k) Applications Submitted by REZA JALINOUS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K060847
03/28/2006
MAGSTIM 200-2
MAGSTIM COMPANY US, LLC.
K991583
05/07/1999
NEUROSIGN 400, 4 CHANNEL MOTOR NERVE MONITOR
THE MAGSTIM COMPANY LTD.
K992911
08/30/1999
MAGSTIM RAPID
MAGSTIM CORPORATION US
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