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FDA 510(k) Application Details - K991583
Device Classification Name
Stimulator, Nerve
More FDA Info for this Device
510(K) Number
K991583
Device Name
Stimulator, Nerve
Applicant
THE MAGSTIM COMPANY LTD.
730 FIFTH AVE, 9TH FLOOR
NEW YORK, NY 10019 US
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Contact
REZA JALINOUS
Other 510(k) Applications for this Contact
Regulation Number
874.1820
More FDA Info for this Regulation Number
Classification Product Code
ETN
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More FDA Info for this Product Code
Date Received
05/07/1999
Decision Date
05/19/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
EN - Ear, Nose, & Throat
Review Advisory Committee
EN - Ear, Nose, & Throat
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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