Lisca Development AB
SwedenFDA applicant, unverified
- Devices
- 1
What Lisca Development AB makes
Lisca Development AB manufactures the PIM 1.0 Laser Doppler Perfusion Imager, a device used for assessing blood flow and tissue perfusion in clinical settings.
The PIM 1.0 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
Pim 1.0 Laser Doppler Perfusion Imager Ref K920844
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lisca Development AB have in the registry?
The registry currently lists 1 device for Lisca Development AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lisca Development AB's devices?
Among its 1 most recently registered device, Lisca Development AB has devices listed in FDA 510(k) (1 device).
What risk classes do Lisca Development AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Lisca Development AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lisca Development AB in the registry?
The most recently registered devices listed for Lisca Development AB include PIM 1.0 LASER DOPPLER PERFUSION IMAGER.