Ohio Imaging, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Model 3000 Nuclear Camera Ref K882312
Regimes: 510(k) Registry: 510(k)Prism 1500XP Nuclear Gamma Camera System Ref K945261
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ohio Imaging, Inc. have in the registry?
The registry currently lists 3 devices for Ohio Imaging, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ohio Imaging, Inc.'s devices?
Among its 3 most recently registered devices, Ohio Imaging, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Ohio Imaging, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ohio Imaging, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ohio Imaging, Inc. in the registry?
The most recently registered devices listed for Ohio Imaging, Inc. include PRISM 3000 NUCLEAR GAMMA CAMERA SYSTEM MODIFICATION, MODEL 3000 NUCLEAR CAMERA and PRISM 1500XP NUCLEAR GAMMA CAMERA SYSTEM.