FDA 510(k) Application Details - K023218

Device Classification Name	Needle, Conduction, Anesthetic (W/Wo Introducer)   More FDA Info for this Device
510(K) Number	K023218
Device Name	Needle, Conduction, Anesthetic (W/Wo Introducer)
Applicant	PAJUNK GMBH 5010 NW CRESCENT VALLEY DR. CORVALLIS, OR 97330 US Other 510(k) Applications for this Company
Contact	BURK BRANDT 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	09/26/2002
Decision Date	03/24/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review