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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