Argus Photonics Group
Country not established
- Devices
- 2
What Argus Photonics Group makes
Argus Photonics Group manufactures surgical laser systems, including the ACCU-PULSE 1000 CO₂ Surgical Laser System and the ACCU-PULSE Carbon Dioxide Laser System, designed for precision tissue ablation and cutting in medical procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Accu-Pulse 1000 CO2 Surgical Laser System Ref K983543
Regimes: 510(k) Registry: 510(k)Accu-Pulse Carbon Dioxide Laser System Ref K971830
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Argus Photonics Group have in the registry?
The registry currently lists 2 devices for Argus Photonics Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Argus Photonics Group's devices?
Among its 2 most recently registered devices, Argus Photonics Group has devices listed in FDA 510(k) (2 devices).
What risk classes do Argus Photonics Group's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Argus Photonics Group's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Argus Photonics Group in the registry?
The most recently registered devices listed for Argus Photonics Group include ACCU-PULSE 1000 CO2 SURGICAL LASER SYSTEM and ACCU-PULSE CARBON DIOXIDE LASER SYSTEM.