Centron Corp

FDA Filings

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

FDA Registration(s)
Registration Number3010773581
FEI Number3010773581
NameCENTRON CORPORATION
Owner & OperatorCentron Corporation
Contact Address44 Beolmal-ro, Dongan-gu
Anyang-si KR-41 Gyeonggido 431-804 KR
Official Correspondent
  • Jae Soon Kim
  • 082-31-4227890-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address44 Beolmal-ro, Dongan-gu
Anyang-si Gyeonggido, 14059 KR
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
CENTRON CORPORATION
Blood Collection Monitor CM350 CM3502020-04-27
CENTRON CORPORATION
Data Collection Mixer DCM3000 (BASIC) CM7602020-04-13
CENTRON CORPORATION
Blood Collection Mixer CM735A CM735A2020-04-13
CENTRON CORPORATION
Rapid Seal Tube Sealer SE640 SE6402020-04-13
CENTRON CORPORATION
MacoSeal SE160 SE1602020-04-13
CENTRON CORPORATION
Rapid Seal Tube Sealer SE540 SE5402020-04-13
CENTRON CORPORATION
Rapid Seal Tube Sealer SE340 SE3402020-04-13
CENTRON CORPORATION
Rapid Seal Tube Sealer SE470 SE4702020-04-13
CENTRON CORPORATION
Rapid Seal Tube Sealer SE530 SE5302020-04-13
CENTRON CORPORATION
Rapid Seal Tube Sealer SE330 SE3302020-04-10
CENTRON CORPORATION
DATA COLLECTION MIXER DCM30002013-12-24
CENTRON CORPORATION
BLOOD COLLECTION MONITOR CM3502013-12-24
CENTRON CORPORATION
BLOOD COLLECTION MIXER CM735A2013-12-24
CENTRON CORPORATION
TUBE SEALER SE6402013-12-24
CENTRON CORPORATION
TUBE SEALER SE5402013-12-24
CENTRON CORPORATION
TUBE SEALER SE5302013-12-24
CENTRON CORPORATION
TUBE SEALER SE470RS2013-12-24
CENTRON CORPORATION
TUBE SEALER SE3402013-12-24
CENTRON CORPORATION
TUBE SEALER SE3302013-12-24
CENTRON CORPORATION
TUBE SEALER SE1702013-12-24
CENTRON CORPORATION
TUBE SEALER SE1602013-12-24

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