Viratek, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Viratek, Inc. makes
Viratek, Inc. manufactures aerosol delivery systems for respiratory treatments, including the SPAG PAK and SPAG-2 Aerosol Generator with Virazole. Their portfolio includes the Small Particle Aerosol Generator (SPAG) Model SPAG-2 6000 Series and an Aerosol Delivery Hood, designed for controlled inhalation therapy.
These devices are classified under FDA’s Class I and Class II categories and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Spag Pak Ref K896608
Regimes: 510(k) Registry: 510(k)Spag-2 Aerosol Generator W/Use Of Virazole Ref K870051
Regimes: 510(k) Registry: 510(k)Viratek Small Particle Aerosol Generat Ref K843717
Regimes: 510(k) Registry: 510(k)(Spag) Model Spag-2 6000 Series Ref K871427
Regimes: 510(k) Registry: 510(k)Aerosol Delivery Hood Ref K882396
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Viratek, Inc. have in the registry?
The registry currently lists 5 devices for Viratek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Viratek, Inc.'s devices?
Among its 5 most recently registered devices, Viratek, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Viratek, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Viratek, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Viratek, Inc. in the registry?
The most recently registered devices listed for Viratek, Inc. include SPAG PAK, SPAG-2 AEROSOL GENERATOR W/USE OF VIRAZOLE, VIRATEK SMALL PARTICLE AEROSOL GENERAT and (SPAG) MODEL SPAG-2 6000 SERIES.