FDA 510(k) Application Details - K162951

Device Classification Name	Set, Administration, Intravascular   More FDA Info for this Device
510(K) Number	K162951
Device Name	Set, Administration, Intravascular
Applicant	Douglas Medical Products, Inc. 345 Dunbar Road Mundelein, IL 60060 US Other 510(k) Applications for this Company
Contact	Doug Johnson 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	10/24/2016
Decision Date	07/28/2017
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review