FDA 510(k) Application Details - K070354

Device Classification Name	Needle, Conduction, Anesthetic (W/Wo Introducer)   More FDA Info for this Device
510(K) Number	K070354
Device Name	Needle, Conduction, Anesthetic (W/Wo Introducer)
Applicant	INTERNATIONAL MEDICAL DEVELOPMENT, INC 9202 KELLEY DRIVE P.O. BOX 510 HUNTSVILLE, UT 84317 US Other 510(k) Applications for this Company
Contact	WALTER ZOHMANN 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	02/06/2007
Decision Date	10/05/2007
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