Swisco, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Swisco, Inc. makes
Swisco, Inc. manufactures gas mixtures for medical use, including lung diffusion blends, blood gas formulations, and laser-specific gas combinations. These products are designed to support respiratory therapy, diagnostic blood gas analysis, and laser surgical procedures.
The company’s portfolio is regulated under FDA Class II devices and is listed via the 510(k) premarket notification process. These products are intended for use in the United States.
Catalogue
Lung Diffusion Gas Mixture Ref K882817
Regimes: 510(k) Registry: 510(k)Blood Gas Mixture Ref K882941
Regimes: 510(k) Registry: 510(k)Laser Mixture Ref K882942
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Swisco, Inc. have in the registry?
The registry currently lists 3 devices for Swisco, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Swisco, Inc.'s devices?
Among its 3 most recently registered devices, Swisco, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Swisco, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Swisco, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Swisco, Inc. in the registry?
The most recently registered devices listed for Swisco, Inc. include LUNG DIFFUSION GAS MIXTURE, BLOOD GAS MIXTURE and LASER MIXTURE.