Telectronics and Cordis Pacing Systems
Country not established
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Model 329-701 Bipolar Active-Fixation Lead Ref K883265
Regimes: 510(k) Registry: 510(k)Change To Cathode Powder Specification Ref K881904
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Telectronics and Cordis Pacing Systems have in the registry?
The registry currently lists 3 devices for Telectronics and Cordis Pacing Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Telectronics and Cordis Pacing Systems's devices?
Among its 3 most recently registered devices, Telectronics and Cordis Pacing Systems has devices listed in FDA 510(k) (3 devices).
What risk classes do Telectronics and Cordis Pacing Systems's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Telectronics and Cordis Pacing Systems's devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Telectronics and Cordis Pacing Systems in the registry?
The most recently registered devices listed for Telectronics and Cordis Pacing Systems include MODEL 329-701 BIPOLAR ACTIVE-FIXATION LEAD, CHANGE TO CATHODE POWDER SPECIFICATION and VICOR MODELS 410B & 410D AND MODIFIED 410A PACEMA..