FDA 510(k) Application Details - K143164

Device Classification Name	Catheter, Conduction, Anesthetic   More FDA Info for this Device
510(K) Number	K143164
Device Name	Catheter, Conduction, Anesthetic
Applicant	KIMBERLY-CLARK CORPORATION 43 DISCOVERY, SUITE 100 IRVINE, CA 92618 US Other 510(k) Applications for this Company
Contact	MARIA E WAGNER 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	11/03/2014
Decision Date	12/02/2014
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