Pegasus Airwave, Inc.
Country not established
- Devices
- 4
What Pegasus Airwave, Inc. makes
Pegasus Airwave, Inc. manufactures pressure-relieving mattress systems and wheelchair cushions designed to prevent and manage decubitus ulcers (pressure sores). Their products include the Airwave System, Airwave Plus System, and specialized decubitus ulcer mattresses, which use alternating air pressure to distribute weight and reduce tissue damage.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company’s portfolio is listed in the FDA’s 510(k) database, reflecting compliance with U.S. medical device authorization requirements.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Pegasus Proactive Wheelchair Cushion Ref K930742
Regimes: 510(k) Registry: 510(k)Pegasus Biwave System Ref K933004
Regimes: 510(k) Registry: 510(k)Pegasus Biwave Plus System Ref K944310
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pegasus Airwave, Inc. have in the registry?
The registry currently lists 4 devices for Pegasus Airwave, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pegasus Airwave, Inc.'s devices?
Among its 4 most recently registered devices, Pegasus Airwave, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Pegasus Airwave, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Pegasus Airwave, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pegasus Airwave, Inc. in the registry?
The most recently registered devices listed for Pegasus Airwave, Inc. include PEGASUS AIRWAVE SYST/SPEC MATTRESS DECUBITUS ULCER, PEGASUS PROACTIVE WHEELCHAIR CUSHION, PEGASUS BIWAVE SYSTEM and PEGASUS BIWAVE PLUS SYSTEM.