Tee-Kay Applied Technology
Country not established
- Devices
- 1
What Tee-Kay Applied Technology makes
Tee-Kay Applied Technology manufactures the Texas Interface Pressure Evaluator (TIPE), a device designed to measure and assess interface pressures, particularly in medical or clinical settings where patient positioning and pressure distribution are critical.
The TIPE is classified as a Class I medical device under FDA regulations and is listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Texas Interface Pressure Evaluator-Tipe Ref K831800
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tee-Kay Applied Technology have in the registry?
The registry currently lists 1 device for Tee-Kay Applied Technology. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tee-Kay Applied Technology's devices?
Among its 1 most recently registered device, Tee-Kay Applied Technology has devices listed in FDA 510(k) (1 device).
What risk classes do Tee-Kay Applied Technology's devices fall under?
Among its 1 most recently registered device, the classes recorded for Tee-Kay Applied Technology's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Tee-Kay Applied Technology in the registry?
The most recently registered devices listed for Tee-Kay Applied Technology include TEXAS INTERFACE PRESSURE EVALUATOR-TIPE.