Medtrek Corp.
Country not established
- Devices
- 1
What Medtrek Corp. makes
Medtrek Corp. manufactures PowerTrek Instruments, a line of Class II medical devices designed for diagnostic or procedural use in clinical settings.
These devices are regulated under the FDA’s 510(k) pathway and are listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Powertrek Instruments Ref K972057
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtrek Corp. have in the registry?
The registry currently lists 1 device for Medtrek Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtrek Corp.'s devices?
Among its 1 most recently registered device, Medtrek Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Medtrek Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtrek Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtrek Corp. in the registry?
The most recently registered devices listed for Medtrek Corp. include POWERTREK INSTRUMENTS.