Theratek, Inc.
Country not established
- Devices
- 1
What Theratek, Inc. makes
Theratek, Inc. manufactures the Kensey Catheter, a medical device designed for specific vascular or drainage applications in clinical settings.
The Kensey Catheter is classified as a Class II device under FDA regulations and is authorised through the 510(k) clearance process. The company is based in the United States.
Catalogue
Kensey Catheter Ref K880194
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Theratek, Inc. have in the registry?
The registry currently lists 1 device for Theratek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Theratek, Inc.'s devices?
Among its 1 most recently registered device, Theratek, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Theratek, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Theratek, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Theratek, Inc. in the registry?
The most recently registered devices listed for Theratek, Inc. include KENSEY CATHETER.