Hepatiq, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Hepatiq, LLC makes
Hepatiq, LLC manufactures the HEPATIQ and HEPATIQ 1.1 devices, which are designed for diagnostic or monitoring purposes related to liver health, specifically targeting hepatitis-related assessments.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Hepatiq Ref K142891
Regimes: 510(k) Registry: 510(k)Hepatiq 1.1 Ref K161188
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hepatiq, LLC have in the registry?
The registry currently lists 2 devices for Hepatiq, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hepatiq, LLC's devices?
Among its 2 most recently registered devices, Hepatiq, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Hepatiq, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hepatiq, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hepatiq, LLC in the registry?
The most recently registered devices listed for Hepatiq, LLC include HEPATIQ and HEPATIQ 1.1.