Biox Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Biox Technology, Inc. makes
Biox Technology, Inc. makes oximeters for critical care use, including the BTI BIOX III OXIMETER CRITICAL CAREUNI and the BIOX III models.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Bti Biox Iii Oximeter Critical Careuni Ref K833826
Regimes: 510(k) Registry: 510(k)Biox Iii Ref K820110
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biox Technology, Inc. have in the registry?
The registry currently lists 2 devices for Biox Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biox Technology, Inc.'s devices?
Among its 2 most recently registered devices, Biox Technology, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Biox Technology, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Biox Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biox Technology, Inc. in the registry?
The most recently registered devices listed for Biox Technology, Inc. include BTI BIOX III OXIMETER CRITICAL CAREUNI and BIOX III.