Elecath
Country not established
- Devices
- 1
What Elecath makes
Elecath manufactures the Pacemate Flow Directed Thermal Dilution Catheter, a device used for measuring cardiac output by thermal dilution methods in clinical settings.
The Pacemate is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Pacemate Flow Directed Thermal Dilution Catheter Ref K900317
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Elecath have in the registry?
The registry currently lists 1 device for Elecath. Devices recorded under merged duplicate company entries are counted once.
Which registries list Elecath's devices?
Among its 1 most recently registered device, Elecath has devices listed in FDA 510(k) (1 device).
What risk classes do Elecath's devices fall under?
Among its 1 most recently registered device, the classes recorded for Elecath's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Elecath in the registry?
The most recently registered devices listed for Elecath include PACEMATE FLOW DIRECTED THERMAL DILUTION CATHETER.