Precision Robotics (Hong Kong) Limited
Country not established
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
SIRIUS Endoscope System (PR-SI-1230) Ref K250939
Regimes: 510(k) Registry: 510(k)SIRIUS Endoscope System Ref K221642
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Precision Robotics (Hong Kong) Limited have in the registry?
The registry currently lists 2 devices for Precision Robotics (Hong Kong) Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Precision Robotics (Hong Kong) Limited's devices?
Among its 2 most recently registered devices, Precision Robotics (Hong Kong) Limited has devices listed in FDA 510(k) (2 devices).
What risk classes do Precision Robotics (Hong Kong) Limited's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Precision Robotics (Hong Kong) Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Precision Robotics (Hong Kong) Limited in the registry?
The most recently registered devices listed for Precision Robotics (Hong Kong) Limited include SIRIUS Endoscope System (PR-SI-1230) and SIRIUS Endoscope System.