Laserguide
Country not established
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Surgi-Light Nd:yag Laser For Urological Use Ref K880071
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Surgi-Light Dispos.fiberoptic Del/Sys Gi/Uro Use Ref K873892
Regimes: 510(k) Registry: 510(k)Light-Spot Fiberoptic Laser Handpiece Ref K873664
Regimes: 510(k) Registry: 510(k)Light-Touch Fiberoptic Microcontact Probe Ref K873571
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Laserguide have in the registry?
The registry currently lists 5 devices for Laserguide. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laserguide's devices?
Among its 5 most recently registered devices, Laserguide has devices listed in FDA 510(k) (5 devices).
What risk classes do Laserguide's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Laserguide's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Laserguide in the registry?
The most recently registered devices listed for Laserguide include SURGI-LIGHT ND:YAG LASER FOR UROLOGICAL USE, SURGI-LIGHT DISPOSABLE SYSTEM FOR PULMONOLOGY USE, SURGI-LIGHT DISPOS.FIBEROPTIC DEL/SYS GI/URO USE and LIGHT-SPOT FIBEROPTIC LASER HANDPIECE.