GE Healthcare Surgery GE Oec Medical Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What GE Healthcare Surgery GE Oec Medical Systems, Inc. makes
The company manufactures mobile C-arm fluoroscopy systems, including the OEC 9900 ELITE for advanced intraoperative imaging and the OEC BRIVO series (865 ADVANCE, 785 ESSENTIAL, 715 PRIME) for surgical and procedural guidance.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Oec 9900 Elite Ref K122234
Regimes: 510(k) Registry: 510(k)Oec 9900 Elite Ref K120613
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ge Healthcare Surgery GE Oec Medical Systems, Inc. have in the registry?
The registry currently lists 3 devices for Ge Healthcare Surgery GE Oec Medical Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ge Healthcare Surgery GE Oec Medical Systems, Inc.'s devices?
Among its 3 most recently registered devices, Ge Healthcare Surgery GE Oec Medical Systems, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Ge Healthcare Surgery GE Oec Medical Systems, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ge Healthcare Surgery GE Oec Medical Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ge Healthcare Surgery GE Oec Medical Systems, Inc. in the registry?
The most recently registered devices listed for Ge Healthcare Surgery GE Oec Medical Systems, Inc. include OEC 9900 ELITE and OEC BRIVO 865 ADVANCE, OEC BRIVO 785 ESSENTIAL, AND OEC BRIVO 715 PRIME.