Nfocus Neuromedical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Nfocus Neuromedical, Inc. makes
Nfocus Neuromedical, Inc. manufactures the ACTA Vessel Occlusion System (VOS), designed for vascular embolization procedures, and the Nfocus Neuromedical Echo Distal Access Catheter, used for guiding and navigating within blood vessels during interventional radiology or neurovascular treatments.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Acta Vessel Occlusion System (Vos) Ref K091952
Regimes: 510(k) Registry: 510(k)Nfocus Neuromedical Echo Distal Access Catheter Ref K090918
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nfocus Neuromedical, Inc. have in the registry?
The registry currently lists 2 devices for Nfocus Neuromedical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nfocus Neuromedical, Inc.'s devices?
Among its 2 most recently registered devices, Nfocus Neuromedical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Nfocus Neuromedical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Nfocus Neuromedical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nfocus Neuromedical, Inc. in the registry?
The most recently registered devices listed for Nfocus Neuromedical, Inc. include ACTA VESSEL OCCLUSION SYSTEM (VOS) and NFOCUS NEUROMEDICAL ECHO DISTAL ACCESS CATHETER.