Pegabus Egerton, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 2
What Pegabus Egerton, Ltd. makes
Pegabus Egerton, Ltd. manufactures the PARAGON PORTABLE, a portable medical device, and the ELITE 3 LOW AIR LOSS BED, designed for patient support and pressure redistribution in clinical settings.
These products are classified as Class II devices under FDA regulations and are listed via 510(k) clearance. The company operates from the United States.
Catalogue
Paragon Portable Ref K945041
Regimes: 510(k) Registry: 510(k)Elite 3 Low Air Loss Bed Ref K945042
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pegabus Egerton, Ltd. have in the registry?
The registry currently lists 2 devices for Pegabus Egerton, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pegabus Egerton, Ltd.'s devices?
Among its 2 most recently registered devices, Pegabus Egerton, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Pegabus Egerton, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pegabus Egerton, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pegabus Egerton, Ltd. in the registry?
The most recently registered devices listed for Pegabus Egerton, Ltd. include PARAGON PORTABLE and ELITE 3 LOW AIR LOSS BED.