Bilab
South KoreaFDA applicant, unverified
- Devices
- 1
What Bilab makes
Bilab manufactures the AirTom device, which is a Class II medical device.
The company is based in the US and its products are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
AirTom Ref K222466
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bilab have in the registry?
The registry currently lists 1 device for Bilab. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bilab's devices?
Among its 1 most recently registered device, Bilab has devices listed in FDA 510(k) (1 device).
What risk classes do Bilab's devices fall under?
Among its 1 most recently registered device, the classes recorded for Bilab's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bilab in the registry?
The most recently registered devices listed for Bilab include AirTom.