Gas-Vak
Country not established
- Devices
- 2
What Gas-Vak makes
Gas-Vak manufactures medical sterilizers and ventilators, including the GAS-VAK Model 300 and a combined sterilizer-ventilator unit. These devices use gas sterilization technology for reprocessing medical instruments and equipment, with integrated ventilation capabilities for patient care applications.
The company’s products fall under FDA Class II devices and are listed via 510(k) clearance in the United States. The portfolio is regulated under US medical device laws, with no EU or international listings referenced.
Catalogue
Gas-Vak(R), Model 300 Ref K890438
Regimes: 510(k) Registry: 510(k)Gas-Vak(R) Combination Sterilizer & Ventilator Ref K902906
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gas-Vak have in the registry?
The registry currently lists 2 devices for Gas-Vak. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gas-Vak's devices?
Among its 2 most recently registered devices, Gas-Vak has devices listed in FDA 510(k) (2 devices).
What risk classes do Gas-Vak's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Gas-Vak's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gas-Vak in the registry?
The most recently registered devices listed for Gas-Vak include GAS-VAK(R), MODEL 300 and GAS-VAK(R) COMBINATION STERILIZER & VENTILATOR.