Kevtek Medical Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Kevtek Laser-Stop Endotracheal Tube Laser-Stop Ref K902193
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kevtek Medical Products, Inc. have in the registry?
The registry currently lists 2 devices for Kevtek Medical Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kevtek Medical Products, Inc.'s devices?
Among its 2 most recently registered devices, Kevtek Medical Products, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Kevtek Medical Products, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Kevtek Medical Products, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kevtek Medical Products, Inc. in the registry?
The most recently registered devices listed for Kevtek Medical Products, Inc. include KEVTEK LASER-STOP ENDOTRACHEAL TUBE LASER-STOP and KEVTEK(TM) LASER DRAPE/ORGAN PROTECTOR/EYE SHIELD.