Qualisys Ab

FDA Filings

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

FDA Registration(s)
Registration Number3015786441
FEI Number3015786441
NameQUALISYS AB
Owner & OperatorQualisys AB
Contact AddressKvarnbergsgatan 2
Gothenburg SE-O Vastra Gotalands lan [SE-14] 41105 SE
Official Correspondent
  • Charlotta Smalander
  • 46-31-3369400-9441
US Agent
Importing Logistics Registration
ImporterQualisys North America Inc.
Address1603 Barclay Blvd
Buffalo Grove, IL 60089 UNITED STATES
Phone1 847 7781386
Importer TypeAgent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressKvarnbergsgatan 2
Gothenburg Vastra Gotalands lan [SE-14], 41105 SE
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Qualisys AB
 Qualisys Clinical System 2020-09-10
QUALISYS AB
Qualisys Clinical System (QCS)2019-09-16
Qualisys AB
Qualisys Clinical System2018-08-02

Related Finance Registrations
NCAGE CodeAG98NQUALISYS AB
NCAGE CodeSZY36QUALISYS AB
CAGE CodeAG98NQUALISYS AB
CAGE CodeSZY36QUALISYS AB
SEC0001018715QUALISYS AB
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.