FDA 510(k) Application Details - K191232

Device Classification Name	Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days   More FDA Info for this Device
510(K) Number	K191232
Device Name	Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days
Applicant	C.R. Bard, Inc 605 North 5600 West Salt Lake City, UT 84116 US Other 510(k) Applications for this Company
Contact	Mona Shahrebani Other 510(k) Applications for this Contact
Regulation Number	880.5200   More FDA Info for this Regulation Number
Classification Product Code	FOZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/08/2019
Decision Date	09/18/2019
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