FDA 510(k) Application Details - K032981

Device Classification Name	Needle, Conduction, Anesthetic (W/Wo Introducer)   More FDA Info for this Device
510(K) Number	K032981
Device Name	Needle, Conduction, Anesthetic (W/Wo Introducer)
Applicant	INVAMED TECHNOLOGIES INC. 9955 TITAN PARK CIRCLE LITTLETON, CO 80125 US Other 510(k) Applications for this Company
Contact	TIM DUVALL 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	09/24/2003
Decision Date	04/22/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review