Oec-Diasonics, Inc.
United StatesFDA applicant, unverified
- Devices
- 8
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Uroview Ref K872022
Regimes: 510(k) Registry: 510(k)Uroview Ii Ref K893475
Regimes: 510(k) Registry: 510(k)F.A.S.T. Table Ref K896583
Regimes: 510(k) Registry: 510(k)Uroview 2000, Modification Ref K914446
Regimes: 510(k) Registry: 510(k)9600 Fluoroscopic Imaging System Ref K926056
Regimes: 510(k) Registry: 510(k)Ep 3000 Ref K924879
Regimes: 510(k) Registry: 510(k)Modified Mainframe Of Model 902 Mobile C-Arm Ref K864837
Regimes: 510(k) Registry: 510(k)Angioplus-S Ref K843972
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oec-Diasonics, Inc. have in the registry?
The registry currently lists 8 devices for Oec-Diasonics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oec-Diasonics, Inc.'s devices?
Among its 8 most recently registered devices, Oec-Diasonics, Inc. has devices listed in FDA 510(k) (8 devices).
What risk classes do Oec-Diasonics, Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Oec-Diasonics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oec-Diasonics, Inc. in the registry?
The most recently registered devices listed for Oec-Diasonics, Inc. include UROVIEW, UROVIEW II, F.A.S.T. TABLE and UROVIEW 2000, MODIFICATION.