Cordic Corp.
Country not established
- Devices
- 1
What Cordic Corp. makes
Cordic Corp. manufactures bipolar epicardial leads designed for temporary pacing applications, intended to be placed on the heart surface during surgical procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Temp. Bipolar Epicardial Lead Ref K831645
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cordic Corp. have in the registry?
The registry currently lists 1 device for Cordic Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cordic Corp.'s devices?
Among its 1 most recently registered device, Cordic Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Cordic Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cordic Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cordic Corp. in the registry?
The most recently registered devices listed for Cordic Corp. include TEMP. BIPOLAR EPICARDIAL LEAD.