FDA 510(k) Application Details - K962886

Device Classification Name	Needle, Conduction, Anesthetic (W/Wo Introducer)   More FDA Info for this Device
510(K) Number	K962886
Device Name	Needle, Conduction, Anesthetic (W/Wo Introducer)
Applicant	ISPG, INC. 517 LITCHFIELD RD. NEW MILFORD, CT 06776 US Other 510(k) Applications for this Company
Contact	LORETTA F LUHMAN Other 510(k) Applications for this Contact
Regulation Number	868.5150   More FDA Info for this Regulation Number
Classification Product Code	BSP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/24/1996
Decision Date	10/09/1996
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