Olympus Corp of America
United StatesFDA applicant, unverified
- Devices
- 2
What Olympus Corp of America makes
Olympus Corp of America makes the Olympus HX-20 Series ligating device and urea nitrogen reagent.
These devices are Class II medical devices listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Olympus Hx-20 Series Ligating Device Ref K984255
Regimes: 510(k) Registry: 510(k)Urea Nitrogen Reagent Ref K944250
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Olympus Corp of America have in the registry?
The registry currently lists 2 devices for Olympus Corp of America. Devices recorded under merged duplicate company entries are counted once.
Which registries list Olympus Corp of America's devices?
Among its 2 most recently registered devices, Olympus Corp of America has devices listed in FDA 510(k) (2 devices).
What risk classes do Olympus Corp of America's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Olympus Corp of America's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Olympus Corp of America in the registry?
The most recently registered devices listed for Olympus Corp of America include OLYMPUS HX-20 SERIES LIGATING DEVICE and UREA NITROGEN REAGENT.