Novasom, Inc.
Country not established
- Devices
- 10
What Novasom, Inc. makes
Novasom, Inc. manufactures the ACCUSOM, a medical device designed for diagnostic imaging of the gastrointestinal tract, specifically for assessing esophageal motility and function.
The ACCUSOM is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Accusom Ref K110486
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 808379150
- [email protected]
- Phone
- 4105901823
Frequently asked questions
How many devices does Novasom, Inc. have in the registry?
The registry currently lists 10 devices for Novasom, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Novasom, Inc.'s devices?
Among its 10 most recently registered devices, Novasom, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (9 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Novasom, Inc.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Novasom, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Novasom, Inc. in the registry?
The most recently registered devices listed for Novasom, Inc. include AccuSom 1017-15004-US, AccuSom 1017-50003-US, AccuSom 1017-10001-US and AccuSom NS2010.