Opko Instrumentation, Inc.
Country not established
- Devices
- 1
What Opko Instrumentation, Inc. makes
Opko Instrumentation, Inc. manufactures the OTI-SCAN 3000, a medical imaging device designed for specific diagnostic applications in radiology.
The company’s portfolio is regulated under FDA Class II devices and includes submissions through the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Oti-Scan 3000 Ref K092837
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Opko Instrumentation, Inc. have in the registry?
The registry currently lists 1 device for Opko Instrumentation, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Opko Instrumentation, Inc.'s devices?
Among its 1 most recently registered device, Opko Instrumentation, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Opko Instrumentation, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Opko Instrumentation, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Opko Instrumentation, Inc. in the registry?
The most recently registered devices listed for Opko Instrumentation, Inc. include OTI-SCAN 3000.