Photon Sources
Country not established
- Devices
- 2
What Photon Sources makes
Photon Sources manufactures colposcopically directed laser systems for obstetrics and gynecology, including the OB/GYN Laser Model 920. These devices are designed for targeted tissue ablation or coagulation in gynecological procedures.
The company’s portfolio is regulated under FDA’s Class II device category and requires 510(k) clearance. The devices are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Colposcopically Directed Ob/Gyn Laser Ref K761347
Regimes: 510(k) Registry: 510(k)Ob/Gyn Laser, Model 920 Ref K772023
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Photon Sources have in the registry?
The registry currently lists 2 devices for Photon Sources. Devices recorded under merged duplicate company entries are counted once.
Which registries list Photon Sources's devices?
Among its 2 most recently registered devices, Photon Sources has devices listed in FDA 510(k) (2 devices).
What risk classes do Photon Sources's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Photon Sources's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Photon Sources in the registry?
The most recently registered devices listed for Photon Sources include COLPOSCOPICALLY DIRECTED OB/GYN LASER and OB/GYN LASER, MODEL 920.