Luco Hybrid Osa Appliance, Inc.
CanadaFDA applicant, unverified
- Devices
- 2
What Luco Hybrid Osa Appliance, Inc. makes
Luco Hybrid Osa Appliance, Inc. makes the Luco Hybrid OSA Appliance, a device designed for the treatment of obstructive sleep apnea.
The Luco Hybrid OSA Appliance is classified as a Class II device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
The Luco Hybrid OSA Appliance Ref K160477
Regimes: 510(k) Registry: 510(k)Luco Hybrid Osa Appliance Ref K130797
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Luco Hybrid Osa Appliance, Inc. have in the registry?
The registry currently lists 2 devices for Luco Hybrid Osa Appliance, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Luco Hybrid Osa Appliance, Inc.'s devices?
Among its 2 most recently registered devices, Luco Hybrid Osa Appliance, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Luco Hybrid Osa Appliance, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Luco Hybrid Osa Appliance, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Luco Hybrid Osa Appliance, Inc. in the registry?
The most recently registered devices listed for Luco Hybrid Osa Appliance, Inc. include The Luco Hybrid OSA Appliance and LUCO HYBRID OSA APPLIANCE.