Protectair, Inc.
Country not established
- Devices
- 1
What Protectair, Inc. makes
Protectair, Inc. makes the Goodall Laser Targeting Device.
The Goodall Laser Targeting Device is a Class II medical device listed in the FDA 510(k) registry. Protectair, Inc. is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Goodall Laser Targeting Device Ref K934626
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Protectair, Inc. have in the registry?
The registry currently lists 1 device for Protectair, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Protectair, Inc.'s devices?
Among its 1 most recently registered device, Protectair, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Protectair, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Protectair, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Protectair, Inc. in the registry?
The most recently registered devices listed for Protectair, Inc. include GOODALL LASER TARGETING DEVICE.