Pneumowave, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Pneumowave, Ltd. makes
Pneumowave, Ltd. manufactures the PW-DCM, a diagnostic device used for assessing cardiac mechanics and ventricular function via non-invasive ultrasound imaging.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the US regulatory registry.
Catalogue
Dcm (Pw-Dcm) Ref K243513
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pneumowave, Ltd. have in the registry?
The registry currently lists 1 device for Pneumowave, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pneumowave, Ltd.'s devices?
Among its 1 most recently registered device, Pneumowave, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Pneumowave, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pneumowave, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pneumowave, Ltd. in the registry?
The most recently registered devices listed for Pneumowave, Ltd. include DCM (PW-DCM).