Omni-Glow, Inc.
Country not established
- Devices
- 1
What Omni-Glow, Inc. makes
Omni-Glow, Inc. manufactures infusion pumps and intravenous (IV) sets designed for controlled delivery of fluids and medications in clinical settings.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Infusion Pump & Iv Sets #4000 Ref K832755
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Omni-Glow, Inc. have in the registry?
The registry currently lists 1 device for Omni-Glow, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Omni-Glow, Inc.'s devices?
Among its 1 most recently registered device, Omni-Glow, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Omni-Glow, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Omni-Glow, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Omni-Glow, Inc. in the registry?
The most recently registered devices listed for Omni-Glow, Inc. include INFUSION PUMP & IV SETS #4000.