FDA 510(k) Application Details - K122661

Device Classification Name	Catheter, Conduction, Anesthetic   More FDA Info for this Device
510(K) Number	K122661
Device Name	Catheter, Conduction, Anesthetic
Applicant	VITAL 5 570 RESEARCH PARK WAY SUITE 102 NORTH LOGAN, UT 84341 US Other 510(k) Applications for this Company
Contact	T. WADE FALLIN 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	08/31/2012
Decision Date	02/27/2013
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