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FDA 510(k) Application Details - K030737
Device Classification Name
Neuroimaging Correlation Software For Electroencephalograph Or Magnetoencephalograph
More FDA Info for this Device
510(K) Number
K030737
Device Name
Neuroimaging Correlation Software For Electroencephalograph Or Magnetoencephalograph
Applicant
CTF SYSTEMS (2001), INC.
15-1750 MCLEAN AVE.
PORT COQUITLAM, B.C. V3C 1M9 CA
Other 510(k) Applications for this Company
Contact
DARYL WISDAHL
Other 510(k) Applications for this Contact
Regulation Number
882.1400
More FDA Info for this Regulation Number
Classification Product Code
OLX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/10/2003
Decision Date
10/10/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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