SCIBASE AB

FDA Filings

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

FDA Registration(s)
Registration Number3008285458
FEI Number3008285458
NameSCIBASE AB
Owner & OperatorScibase AB
Contact AddressLandsvagen 39
Sundbyberg SE-AB Stockholms lan [SE-01] 17263 SE
Official Correspondent
  • Simon J Grant
  • 46-72-8874399-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressLandsvagen 39
sundbyberg Stockholms lan [SE-01], 17263 SE
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
SCIBASE AB
Nevisense2020-04-30
Scibase AB
NeviFile kit US 142-00132019-03-04
SCIBASE AB
Nevisense2019-01-14
SCIBASE AB
Nevisense2018-12-11
SCIBASE AB
Nevisense2018-07-13
Scibase AB
Training electrode Sterile - 6 pcs 131-00082018-07-06
Scibase AB
Single Use Electrodes Sterile - 6 pcs 131-00072018-07-06
Scibase AB
Control Unit Battery 521-00012018-07-06
Scibase AB
Test Impedance Tool 590-00022018-07-06
Scibase AB
Probe cable 730-00092018-07-06
Scibase AB
Probe unit 512-00032018-07-06
Scibase AB
Nevisense 511-00012018-07-06
SCIBASE AB
Nevisense2017-07-06
SCIBASE AB
NEVISENSE2017-06-28

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