FDA 510(k) Application Details - K153393

Device Classification Name	More FDA Info for this Device
510(K) Number	K153393
Device Name	PowerMidline Catheter
Applicant	C.R. BARD, INC 605 NORTH 5600 WEST SALT LAKE CITY, UT 84116 US Other 510(k) Applications for this Company
Contact	Casey Coombs Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PND Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/24/2015
Decision Date	06/28/2016
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review