Eko Scann AB
Country not established
- Devices
- 2
What Eko Scann AB makes
Eko Scann AB manufactures medical devices including the DEVETHERM, a device used for temperature monitoring, and the VISCOUNT hematology computer-interface, which facilitates data processing for blood analysis systems.
The company’s portfolio consists of Class II devices, regulated under the FDA’s 510(k) clearance process. These devices are listed in the FDA’s 510(k) registry, and the company is based in the United States.
Catalogue
Devetherm Ref K822873
Regimes: 510(k) Registry: 510(k)Hematology Computer-Interface, Viscount Ref K822823
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eko Scann AB have in the registry?
The registry currently lists 2 devices for Eko Scann AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eko Scann AB's devices?
Among its 2 most recently registered devices, Eko Scann AB has devices listed in FDA 510(k) (2 devices).
What risk classes do Eko Scann AB's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Eko Scann AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eko Scann AB in the registry?
The most recently registered devices listed for Eko Scann AB include DEVETHERM and HEMATOLOGY COMPUTER-INTERFACE, VISCOUNT.