FDA 510(k) Application Details - K051401

Device Classification Name	Catheter, Conduction, Anesthetic   More FDA Info for this Device
510(K) Number	K051401
Device Name	Catheter, Conduction, Anesthetic
Applicant	I-FLOW CORP. 20202 WINDROW DR. LAKE FOREST, CA 92630 US Other 510(k) Applications for this Company
Contact	SHANE NOEHRE Other 510(k) Applications for this Contact
Regulation Number	868.5120   More FDA Info for this Regulation Number
Classification Product Code	BSO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/31/2005
Decision Date	11/30/2005
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