Digiflo, Inc.
Country not established
- Devices
- 1
What Digiflo, Inc. makes
Digiflo, Inc. manufactures the Digiflo Concentrator Analyzer, a device designed for analyzing blood gas and electrolyte concentrations in clinical settings.
The company’s portfolio is regulated under FDA’s Class II designation and requires 510(k) clearance. The device is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Digiflo Concentrator Analyzer Ref K072469
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Digiflo, Inc. have in the registry?
The registry currently lists 1 device for Digiflo, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Digiflo, Inc.'s devices?
Among its 1 most recently registered device, Digiflo, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Digiflo, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Digiflo, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Digiflo, Inc. in the registry?
The most recently registered devices listed for Digiflo, Inc. include DIGIFLO CONCENTRATOR ANALYZER.