FDA 510(k) Application Details - K223101

Device Classification Name	Set, Administration, Intravascular   More FDA Info for this Device
510(K) Number	K223101
Device Name	Set, Administration, Intravascular
Applicant	CareFusion 10020 Pacific Mesa Blvd San Diego, CA 92121 US Other 510(k) Applications for this Company
Contact	Paulina Davis Other 510(k) Applications for this Contact
Regulation Number	880.5440   More FDA Info for this Regulation Number
Classification Product Code	FPA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/30/2022
Decision Date	05/12/2023
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