M. D. Software, Inc.
Country not established
- Devices
- 1
What M. D. Software, Inc. makes
M. D. Software, Inc. develops software programs for interpreting arterial blood gas (ABG) results, assisting clinicians in analyzing and diagnosing respiratory and metabolic conditions based on laboratory measurements.
The company’s portfolio is regulated under FDA’s Class II device classification and is listed via 510(k) premarket notifications. The manufacturer operates from the United States.
Catalogue
Arterial Blood Gas Interpretation Prog Ref K840102
510(k) 510(k)
Frequently asked questions
How many devices does M. D. Software, Inc. have in the registry?
The registry currently lists 1 device for M. D. Software, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list M. D. Software, Inc.'s devices?
Among its 1 most recently registered device, M. D. Software, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do M. D. Software, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for M. D. Software, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from M. D. Software, Inc. in the registry?
The most recently registered devices listed for M. D. Software, Inc. include ARTERIAL BLOOD GAS INTERPRETATION PROG.