Necon Medical, Inc.
Country not established
- Devices
- 1
What Necon Medical, Inc. makes
Necon Medical, Inc. manufactures the TURBO AIR COMPRESSOR 8000, a medical-grade air compressor designed for use in clinical and procedural settings. This device provides compressed air for applications such as pneumatic surgical tools, insufflation, or other medical procedures requiring controlled airflow.
The company’s products fall under Class II regulatory classification in the U.S., with individual devices authorised through FDA 510(k) clearance. The portfolio is listed in the FDA’s regulatory database, and the manufacturer operates from the United States.
Catalogue
Turbo Air Compressor 8000 Ref K883829
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Necon Medical, Inc. have in the registry?
The registry currently lists 1 device for Necon Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Necon Medical, Inc.'s devices?
Among its 1 most recently registered device, Necon Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Necon Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Necon Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Necon Medical, Inc. in the registry?
The most recently registered devices listed for Necon Medical, Inc. include TURBO AIR COMPRESSOR 8000.