Ventipress Oy
FinlandFDA applicant, unverified
- Devices
- 1
What Ventipress Oy makes
Ventipress Oy manufactures the VentiPress 24 and VentiPress 14, which are pressure ventilators designed for mechanical respiratory support in clinical settings.
The company’s ventilators are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Ventipress 24 And 14 Pressure Ventilator Ref K893950
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ventipress OY have in the registry?
The registry currently lists 1 device for Ventipress OY. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ventipress OY's devices?
Among its 1 most recently registered device, Ventipress OY has devices listed in FDA 510(k) (1 device).
What risk classes do Ventipress OY's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ventipress OY's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ventipress OY in the registry?
The most recently registered devices listed for Ventipress OY include VENTIPRESS 24 AND 14 PRESSURE VENTILATOR.