Med*Ex Diagnostics of Canada, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Med*Ex Diagnostics of Canada, Inc. makes
Med*Ex Diagnostics of Canada, Inc. manufactures the DYNATRAC, a diagnostic device designed for measuring dynamic respiratory mechanics and lung function in clinical settings.
The company’s portfolio is regulated under FDA’s Class II device classification, with the DYNATRAC authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Dynatrac Ref K872974
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Med*Ex Diagnostics of Canada, Inc. have in the registry?
The registry currently lists 1 device for Med*Ex Diagnostics of Canada, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Med*Ex Diagnostics of Canada, Inc.'s devices?
Among its 1 most recently registered device, Med*Ex Diagnostics of Canada, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Med*Ex Diagnostics of Canada, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Med*Ex Diagnostics of Canada, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Med*Ex Diagnostics of Canada, Inc. in the registry?
The most recently registered devices listed for Med*Ex Diagnostics of Canada, Inc. include DYNATRAC.