Respinova, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Respinova, Ltd. makes
Respinova, Ltd. manufactures the Pulsehaler, a Class II medical device.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pulsehaler Ref K203378
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Respinova, Ltd. have in the registry?
The registry currently lists 1 device for Respinova, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Respinova, Ltd.'s devices?
Among its 1 most recently registered device, Respinova, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Respinova, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Respinova, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Respinova, Ltd. in the registry?
The most recently registered devices listed for Respinova, Ltd. include Pulsehaler.