Biometric Research Institute, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Biometric Research Institute, Inc. makes
Biometric Research Institute, Inc. manufactures medical devices for monitoring and measuring physiological parameters, including a catheter-based oxygen and carbon monoxide filtration system (Model OXI/CO FILA. THERMO. CATH.) and a cardiac output measurement device (Model INTERFLO/1). These products are designed for use in critical care and intraoperative settings to assess gas exchange and hemodynamic function.
The company’s portfolio consists of Class II devices as classified by the FDA, with regulatory submissions supported through 510(k) clearances. These devices are listed under the U.S. regulatory framework and are intended for use within the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Interflo Medical Model Interflo/1 Cardiac Output Ref K902628
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biometric Research Institute, Inc. have in the registry?
The registry currently lists 2 devices for Biometric Research Institute, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biometric Research Institute, Inc.'s devices?
Among its 2 most recently registered devices, Biometric Research Institute, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Biometric Research Institute, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Biometric Research Institute, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biometric Research Institute, Inc. in the registry?
The most recently registered devices listed for Biometric Research Institute, Inc. include INTERFLO MEDICAL MODEL OXI/CO FILA. THERMO. CATH. and INTERFLO MEDICAL MODEL INTERFLO/1 CARDIAC OUTPUT.