FDA 510(k) Application Details - K001692

Device Classification Name	Device, Nerve Conduction Velocity Measurement   More FDA Info for this Device
510(K) Number	K001692
Device Name	Device, Nerve Conduction Velocity Measurement
Applicant	NEUROSOFT, INC. 5700 CROMO, SUITE 100 EL PASO, TX 79912 US Other 510(k) Applications for this Company
Contact	DAVID B JONES Other 510(k) Applications for this Contact
Regulation Number	882.1550   More FDA Info for this Regulation Number
Classification Product Code	JXE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/02/2000
Decision Date	11/24/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review