Jillian Ikovich

FDA Filings

This page includes the latest FDA filings for Jillian Ikovich. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3014663754
FEI Number3014663754
NameJillian ikovich
Owner & OperatorVYGON S A
Contact Address5-11 RUE ADELINE --
ECOUEN FR-NOTA 95440 FR
Official Correspondent
  • Jillian J Mikovich
  • 33-139-926363-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2750 Morris Road
Lansdale, PA 19446 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Jillian ikovich [VYGON S A]
Vygon Double Lumen Umbilical Catheter2012-03-26
Jillian ikovich [VYGON S A]
Vygon XRO PVC Venous/Arterial Umbilical Catheter2012-03-26
Jillian ikovich [VYGON S A]
Vygon PVC XRO Venous/Arterial Umbilical Catheter2008-02-02
Jillian ikovich [VYGON S A]
Vygon PVC Umbilical Catheter2008-02-02

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