Nelipak Phoenix

FDA Filings

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

FDA Registration(s)
Registration Number3012137049
FEI Number3012137049
NameNELIPAK PHOENIX
Owner & OperatorNelipak Phoenix
Contact Address3720 West Washington Street
Phoenix AZ 85009 US
Official Correspondent
  • Rolando Salas
  • 1-401-9462699-7114
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3720 West Washington Street
Phoenix, AZ 85009 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
NELIPAK PHOENIX
Light Handle Cover2017-08-22

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