Sentek, Inc.
Country not established
- Devices
- 1
What Sentek, Inc. makes
Sentek, Inc. manufactures the REVISED T-SCAN SYSTEM, a diagnostic device used for electrophysiological testing, specifically for assessing nerve conduction and muscle response.
The REVISED T-SCAN SYSTEM is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Revised T-Scan System Ref K870032
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sentek, Inc. have in the registry?
The registry currently lists 1 device for Sentek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sentek, Inc.'s devices?
Among its 1 most recently registered device, Sentek, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sentek, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sentek, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Sentek, Inc. in the registry?
The most recently registered devices listed for Sentek, Inc. include REVISED T-SCAN SYSTEM.