Pulsecor Limited
Country not established
- Devices
- 1
What Pulsecor Limited makes
Pulsecor Limited manufactures the Cardioscope, a medical device designed for cardiac monitoring and diagnostic purposes, likely used in clinical or emergency settings to assess heart function and rhythm.
The Cardioscope is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Cardioscope Ref K121266
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pulsecor Limited have in the registry?
The registry currently lists 1 device for Pulsecor Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pulsecor Limited's devices?
Among its 1 most recently registered device, Pulsecor Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Pulsecor Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pulsecor Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pulsecor Limited in the registry?
The most recently registered devices listed for Pulsecor Limited include CARDIOSCOPE.