Dwl Elektronische Systeme GmbH
GermanyFDA 510(k) applicant, unverified
- Devices
- 1
What Dwl Elektronische Systeme GmbH makes
Dwl Elektronische Systeme GmbH manufactures the HEMO-DOP, a device designed for measuring and analyzing blood flow dynamics in peripheral arteries, likely used in vascular diagnostics.
The HEMO-DOP is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Hemo-Dop Ref K041915
510(k) 510(k)
Frequently asked questions
How many devices does Dwl Elektronische Systeme GmbH have in the registry?
The registry currently lists 1 device for Dwl Elektronische Systeme GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dwl Elektronische Systeme GmbH's devices?
Among its 1 most recently registered device, Dwl Elektronische Systeme GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Dwl Elektronische Systeme GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dwl Elektronische Systeme GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dwl Elektronische Systeme GmbH in the registry?
The most recently registered devices listed for Dwl Elektronische Systeme GmbH include HEMO-DOP.