Intertronic, Inc.
Country not established
- Devices
- 1
What Intertronic, Inc. makes
Intertronic, Inc. manufactures the RHINOTEST MP, a diagnostic device designed for nasal airflow testing to assess sinus and nasal passage function.
The RHINOTEST MP is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Rhinotest Mp Ref K853024
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intertronic, Inc. have in the registry?
The registry currently lists 1 device for Intertronic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intertronic, Inc.'s devices?
Among its 1 most recently registered device, Intertronic, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Intertronic, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Intertronic, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intertronic, Inc. in the registry?
The most recently registered devices listed for Intertronic, Inc. include RHINOTEST MP.