Nexsys Electronics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Nexsys Electronics, Inc. makes
Nexsys Electronics, Inc. manufactures MEDIPACS, a picture archiving and communication system (PACS) for digital medical imaging, and MEDWEB ADVANCED 3D WEB PACS, a web-based PACS solution designed for 3D imaging data storage, retrieval, and distribution.
These products are regulated under FDA Class I and Class II designations, with the MEDWEB ADVANCED 3D WEB PACS subject to 510(k) clearance via the FDA’s premarket notification process. The company is based in the United States.
Catalogue
Medipacs Ref K950413
Regimes: 510(k) Registry: 510(k)Medweb Advanced 3D Web Pacs Ref K063221
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nexsys Electronics, Inc. have in the registry?
The registry currently lists 2 devices for Nexsys Electronics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nexsys Electronics, Inc.'s devices?
Among its 2 most recently registered devices, Nexsys Electronics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Nexsys Electronics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Nexsys Electronics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nexsys Electronics, Inc. in the registry?
The most recently registered devices listed for Nexsys Electronics, Inc. include MEDIPACS and MEDWEB ADVANCED 3D WEB PACS.