Wm.I.Kern & Co., Inc.
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pbi Multilase D Copper Vapor Laser Ref K920004
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wm.I.Kern & Co., Inc. have in the registry?
The registry currently lists 1 device for Wm.I.Kern & Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wm.I.Kern & Co., Inc.'s devices?
Among its 1 most recently registered device, Wm.I.Kern & Co., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Wm.I.Kern & Co., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wm.I.Kern & Co., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wm.I.Kern & Co., Inc. in the registry?
The most recently registered devices listed for Wm.I.Kern & Co., Inc. include PBI MULTILASE D COPPER VAPOR LASER.