Spectrica
CanadaFDA applicant, unverified
- Devices
- 1
What Spectrica makes
Spectrica manufactures the CYCLONE (Model MAICAM 180), a medical device designed for aerosolized drug delivery in respiratory therapy applications.
The CYCLONE is classified as a Class II device under FDA regulations and is listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Cyclone, Model Maicam 180 Ref K060486
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spectrica have in the registry?
The registry currently lists 1 device for Spectrica. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spectrica's devices?
Among its 1 most recently registered device, Spectrica has devices listed in FDA 510(k) (1 device).
What risk classes do Spectrica's devices fall under?
Among its 1 most recently registered device, the classes recorded for Spectrica's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spectrica in the registry?
The most recently registered devices listed for Spectrica include CYCLONE, MODEL MAICAM 180.