FDA 510(k) Application Details - K960663

Device Classification Name	Block, Bite   More FDA Info for this Device
510(K) Number	K960663
Device Name	Block, Bite
Applicant	B & B MEDICAL TECHNOLOGIES, INC. P.O. BOX 1503 ORANGEVALE, CA 95662 US Other 510(k) Applications for this Company
Contact	JOHN D CALEBAUGH RRT,RCP Other 510(k) Applications for this Contact
Regulation Number	882.5070   More FDA Info for this Regulation Number
Classification Product Code	JXL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/16/1996
Decision Date	05/17/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review