Nanthealth, Inc.
Country not established
- Devices
- 1
What Nanthealth, Inc. makes
Nanthealth, Inc. manufactures the Omics Core, a diagnostic device designed for genomic analysis and molecular testing to support clinical decision-making.
The Omics Core is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Omics Core Ref K190661
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nanthealth, Inc. have in the registry?
The registry currently lists 1 device for Nanthealth, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nanthealth, Inc.'s devices?
Among its 1 most recently registered device, Nanthealth, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Nanthealth, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Nanthealth, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nanthealth, Inc. in the registry?
The most recently registered devices listed for Nanthealth, Inc. include Omics Core.