FDA 510(k) Application Details - K960100

Device Classification Name	Anesthesia Conduction Kit   More FDA Info for this Device
510(K) Number	K960100
Device Name	Anesthesia Conduction Kit
Applicant	SPINAL SPECIALTIES, INC. 4230 CENTERGATE SAN ANTONIO, TX 78217 US Other 510(k) Applications for this Company
Contact	MICHAEL WAKELY Other 510(k) Applications for this Contact
Regulation Number	868.5140   More FDA Info for this Regulation Number
Classification Product Code	CAZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/11/1996
Decision Date	04/24/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review