FDA 510(k) Application Details - K170595

Device Classification Name	Set, Administration, Intravascular   More FDA Info for this Device
510(K) Number	K170595
Device Name	Set, Administration, Intravascular
Applicant	B. Braun Medical Inc. 901 Macon Blvd Allentown, PA 18109 US Other 510(k) Applications for this Company
Contact	Nancy Skocypec 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	02/28/2017
Decision Date	11/07/2017
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