Vabar Corp.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Colostomy Enema Device Ref K790749
Regimes: 510(k) Registry: 510(k)Colostomy Device W/ Pressure Lid Ref K790750
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vabar Corp. have in the registry?
The registry currently lists 2 devices for Vabar Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vabar Corp.'s devices?
Among its 2 most recently registered devices, Vabar Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Vabar Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Vabar Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vabar Corp. in the registry?
The most recently registered devices listed for Vabar Corp. include COLOSTOMY ENEMA DEVICE and COLOSTOMY DEVICE W/ PRESSURE LID.