Optiway, Inc.
Country not established
- Devices
- 1
What Optiway, Inc. makes
Optiway, Inc. manufactures the CORSAIRE, a medical device designed for use in specific surgical procedures, likely within the cardiovascular or vascular domain based on the device name.
The CORSAIRE is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Corsaire Ref K982750
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Optiway, Inc. have in the registry?
The registry currently lists 1 device for Optiway, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Optiway, Inc.'s devices?
Among its 1 most recently registered device, Optiway, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Optiway, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Optiway, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Optiway, Inc. in the registry?
The most recently registered devices listed for Optiway, Inc. include CORSAIRE.