Centron Technologies Inc

FDA Filings

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

Centron Technologies Inc holds import registrations or U.S. agent authorizations in conjunction with the following organizations:

FDA Registration(s)
Registration Number3005824261
FEI Number3005824261
NameCENTRON TECHNOLOGIES, INC.
Owner & OperatorCENTRON TECHNOLOGIES, INC.
Contact Address1308 Edgewood Road, F1
Havertown PA 19083 US
Official Correspondent
  • CHUNG KEUN - GIM
  • x-610-4461310-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1308 Edgewood Road
Havertown, PA 19083 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
CENTRON TECHNOLOGIES, INC.
DATA COLLECTION MIXER: DCM 30002004-12-06
CENTRON TECHNOLOGIES, INC.
BLOOD COLLECTION MONITOR: CM3502004-12-06
CENTRON TECHNOLOGIES, INC.
BLOOD COLLECTION MIXER: CM735A2004-12-06
CENTRON TECHNOLOGIES, INC.
TUBE SEALER: SE6402004-12-06
CENTRON TECHNOLOGIES, INC.
TUBE SEALER: SE5402004-12-06
CENTRON TECHNOLOGIES, INC.
TUBE SEALER: SE5302004-12-06
CENTRON TECHNOLOGIES, INC.
TUBE SEALER: SE470RS2004-12-06
CENTRON TECHNOLOGIES, INC.
TUBE SEALER: SE3402004-12-06
CENTRON TECHNOLOGIES, INC.
TUBE SEALER: SE3302004-12-06
CENTRON TECHNOLOGIES, INC.
TUBE SEALER: SE1602004-12-06

Related Finance Registrations
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.