FDA 510(k) Application Details - K962317

Device Classification Name	Magnetoencephalograph   More FDA Info for this Device
510(K) Number	K962317
Device Name	Magnetoencephalograph
Applicant	BIOMAGNETIC TECHNOLOGIES, INC. 9727 PACIFIC HEIGHTS BLVD. SAN DIEGO, CA 92121-3719 US Other 510(k) Applications for this Company
Contact	EUGENE C HIRSCHKOFF, PH.D. Other 510(k) Applications for this Contact
Regulation Number	882.1400   More FDA Info for this Regulation Number
Classification Product Code	OLY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/17/1996
Decision Date	05/07/1997
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