Altaravision, Inc.
Country not established
- Devices
- 2
What Altaravision, Inc. makes
Altaravision, Inc. manufactures the NDOHD High Definition Imaging System, a device designed for high-definition optical imaging applications in medical settings.
The NDOHD High Definition Imaging System is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Registry: GUDID
NDOHD High Definition Imaging System (NDOHD) Ref K190420
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 064561659
- [email protected]
- Phone
- 8773901887
Frequently asked questions
How many devices does Altaravision, Inc. have in the registry?
The registry currently lists 2 devices for Altaravision, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Altaravision, Inc.'s devices?
Among its 2 most recently registered devices, Altaravision, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Altaravision, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Altaravision, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Altaravision, Inc. in the registry?
The most recently registered devices listed for Altaravision, Inc. include NDOHD High Definition Imaging System (NDOHD) 2.0 and NDOHD High Definition Imaging System (NDOHD).