Oncosoft Inc.
South KoreaFDA applicant, unverified FDA FEI 3036758982
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
OncoStudio Ref K260528
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3036758982
- Address
- 37 Myeongmul-gil Seodaemun-gu, Seoul
Frequently asked questions
How many devices does Oncosoft Inc. have in the registry?
The registry currently lists 1 device for Oncosoft Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oncosoft Inc.'s devices?
Among its 1 most recently registered device, Oncosoft Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Oncosoft Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Oncosoft Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oncosoft Inc. in the registry?
The most recently registered devices listed for Oncosoft Inc. include OncoStudio.