Cooper Lasersonics, Inc.
Also registered as Copper Lasersonics, Inc.
United StatesFDA applicant, unverified
- Devices
- 55
Catalogue
Search and filter all 55 devicesDeviceDevice · Authorizations Verified Status Regime Registry Class
CO2 Fiberoptic Delivery System/Bronchoscopic Use Ref K862835
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Model 4000 Nd:yag Laser For Hemorrhage Control Ref K844440
Regimes: 510(k) Registry: 510(k)Laser Benign & Malignant Pulmonary Obstructions- Ref K850432
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Showing 51-55 of 55