Omni-Flow, Inc.
Country not established
- Devices
- 1
What Omni-Flow, Inc. makes
Omni-Flow, Inc. manufactures the Omni-Flow Therapist Infusion Management System, a device designed for managing and monitoring intravenous infusions in clinical settings. It integrates infusion control, patient monitoring, and data logging to support precise fluid administration and patient care.
The company’s infusion management system is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The device is developed and distributed from the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Omni-Flow, Inc. have in the registry?
The registry currently lists 1 device for Omni-Flow, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Omni-Flow, Inc.'s devices?
Among its 1 most recently registered device, Omni-Flow, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Omni-Flow, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Omni-Flow, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Omni-Flow, Inc. in the registry?
The most recently registered devices listed for Omni-Flow, Inc. include THE OMNI-FLOW THERAPIST INFUSION MANAGEMENT SYSTEM.