Opap, Inc.
Country not established
- Devices
- 1
What Opap, Inc. makes
Opap, Inc. manufactures the OPAP, a device designed for obstructive sleep apnea treatment through non-invasive positive airway pressure therapy.
The OPAP is classified as a Class II medical device in the US and is listed under FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Opap Ref K991926
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Opap, Inc. have in the registry?
The registry currently lists 1 device for Opap, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Opap, Inc.'s devices?
Among its 1 most recently registered device, Opap, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Opap, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Opap, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Opap, Inc. in the registry?
The most recently registered devices listed for Opap, Inc. include OPAP.