Plexus Medical
Country not established
- Devices
- 3
What Plexus Medical makes
Plexus Medical manufactures electrophysiological mapping and ablation catheters, including the PLEXUS/1000 series for general cardiac mapping and the PLEXUS/3000/P/3500 systems for advanced atrial fibrillation ablation procedures. The P/2000 is designed for precision catheter navigation in electrophysiology studies.
These devices are classified as Class II under FDA regulations and are authorised via 510(k) clearance. The company is based in the United States.
Catalogue
Plexus/1000 Ref K943353
Regimes: 510(k) Registry: 510(k)Plexus/3000 (P/3000), Plexus/3500 (P/3500) Ref K952610
Regimes: 510(k) Registry: 510(k)P/2000 Ref K944411
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Plexus Medical have in the registry?
The registry currently lists 3 devices for Plexus Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Plexus Medical's devices?
Among its 3 most recently registered devices, Plexus Medical has devices listed in FDA 510(k) (3 devices).
What risk classes do Plexus Medical's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Plexus Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Plexus Medical in the registry?
The most recently registered devices listed for Plexus Medical include PLEXUS/1000, PLEXUS/3000 (P/3000), PLEXUS/3500 (P/3500) and P/2000.