Neoguide Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Neoguide Endoscopy System Ref K070622
Regimes: 510(k) Registry: 510(k)Navigator Endoscopy System Ref K052930
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neoguide Systems, Inc. have in the registry?
The registry currently lists 2 devices for Neoguide Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neoguide Systems, Inc.'s devices?
Among its 2 most recently registered devices, Neoguide Systems, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Neoguide Systems, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Neoguide Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neoguide Systems, Inc. in the registry?
The most recently registered devices listed for Neoguide Systems, Inc. include NEOGUIDE ENDOSCOPY SYSTEM and NAVIGATOR ENDOSCOPY SYSTEM.