New Wave Surgical Corporation
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Defogging Heated Endoscope Lens Protector (Dhelp); Defogging Endoscope Lens Protector (Delp) Ref K062779
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does New Wave Surgical Corporation have in the registry?
The registry currently lists 1 device for New Wave Surgical Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list New Wave Surgical Corporation's devices?
Among its 1 most recently registered device, New Wave Surgical Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do New Wave Surgical Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for New Wave Surgical Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from New Wave Surgical Corporation in the registry?
The most recently registered devices listed for New Wave Surgical Corporation include DEFOGGING HEATED ENDOSCOPE LENS PROTECTOR (DHELP); DEFOGGING ENDOSCOPE LENS PROTECTOR (DELP).