Modular Diagnostic Systems, Inc.
Country not established
- Devices
- 1
What Modular Diagnostic Systems, Inc. makes
Modular Diagnostic Systems, Inc. manufactures the PROFILE ONE OMNI, a diagnostic device designed for clinical testing and analysis in laboratory settings.
The PROFILE ONE OMNI is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Profile One Omni Ref K882559
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Modular Diagnostic Systems, Inc. have in the registry?
The registry currently lists 1 device for Modular Diagnostic Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Modular Diagnostic Systems, Inc.'s devices?
Among its 1 most recently registered device, Modular Diagnostic Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Modular Diagnostic Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Modular Diagnostic Systems, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Modular Diagnostic Systems, Inc. in the registry?
The most recently registered devices listed for Modular Diagnostic Systems, Inc. include PROFILE ONE OMNI.