Monitor/Demlar
Country not established
- Devices
- 1
What Monitor/Demlar makes
Monitor/Demlar makes the MODEL 20-P EXTENDED HIGH FREQUENCY AUDIOMETER, a device used for assessing hearing sensitivity at elevated frequencies beyond standard audiometric ranges.
This device is classified as Class II and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Model 20-P Extended High Frequency Audiometer Ref K890497
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Monitor/Demlar have in the registry?
The registry currently lists 1 device for Monitor/Demlar. Devices recorded under merged duplicate company entries are counted once.
Which registries list Monitor/Demlar's devices?
Among its 1 most recently registered device, Monitor/Demlar has devices listed in FDA 510(k) (1 device).
What risk classes do Monitor/Demlar's devices fall under?
Among its 1 most recently registered device, the classes recorded for Monitor/Demlar's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Monitor/Demlar in the registry?
The most recently registered devices listed for Monitor/Demlar include MODEL 20-P EXTENDED HIGH FREQUENCY AUDIOMETER.