Baronova, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
BAROnova Access Sheath Kit Ref K191078
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Baronova, Inc. have in the registry?
The registry currently lists 4 devices for Baronova, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Baronova, Inc.'s devices?
Among its 4 most recently registered devices, Baronova, Inc. has devices listed in FDA 510(k) (3 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Baronova, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Baronova, Inc.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Baronova, Inc. in the registry?
The most recently registered devices listed for Baronova, Inc. include BAROnova Access Sheath Kit, BAROnova Retrieval Kit, BAROnova Overtube, BAROnova Endoscope Cap, BAROnova Insufflation System, BAROnova Accessory Kit and TransPyloric Shuttle/TransPyloric Shuttle Delivery Device.