Hema Metrics, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Hema Metrics, LLC makes
Hema Metrics, LLC develops CRIT-LINE Anemia Management Software, a digital tool designed to assist in monitoring and managing anemia in clinical settings by providing automated alerts and patient tracking features.
The company’s portfolio is regulated under FDA Class I devices and is listed via 510(k) premarket notifications. The manufacturer is based in the United States.
Catalogue
Crit-Line Monitor Iii Tqa (Clm Tqa) Ref K011741
Regimes: 510(k) Registry: 510(k)Crit-Line Anemia Management Software Ref K093834
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hema Metrics, LLC have in the registry?
The registry currently lists 2 devices for Hema Metrics, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hema Metrics, LLC's devices?
Among its 2 most recently registered devices, Hema Metrics, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Hema Metrics, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hema Metrics, LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hema Metrics, LLC in the registry?
The most recently registered devices listed for Hema Metrics, LLC include CRIT-LINE MONITOR III TQA (CLM TQA) and CRIT-LINE ANEMIA MANAGEMENT SOFTWARE.