FDA 510(k) Application Details - K181208

Device Classification Name	More FDA Info for this Device
510(K) Number	K181208
Device Name	Vygon Midline 3 Fr SL Catheter; Vygon Midline 4 Fr SL Catheter; Vygon Midline 5 Fr DL Catheter
Applicant	Vygon USA 2750 Morris Rd Suite A200 Lansdale, PA 19460 US Other 510(k) Applications for this Company
Contact	Jillian Mikovich 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	05/07/2018
Decision Date	11/02/2018
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