Nebel, Inc.
Country not established
- Devices
- 1
What Nebel, Inc. makes
Nebel, Inc. manufactures the CAP-AID (Improved), a Class I medical device designed for use in respiratory care, specifically for improving airway management or ventilation support in patients.
The CAP-AID (Improved) is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Cap-Aid (Improved) Ref K964580
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nebel, Inc. have in the registry?
The registry currently lists 1 device for Nebel, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nebel, Inc.'s devices?
Among its 1 most recently registered device, Nebel, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Nebel, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Nebel, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Nebel, Inc. in the registry?
The most recently registered devices listed for Nebel, Inc. include CAP-AID (IMPROVED).